Prazosin Hydrochloride


Mylan Pharmaceuticals Inc.
Human Prescription Drug
NDC 0378-1101
Prazosin Hydrochloride is a drug for further processing labeled by 'Mylan Pharmaceuticals Inc.'. National Drug Code (NDC) number for Prazosin Hydrochloride is 0378-1101. This drug is available in dosage form of Capsule. The names of the active, medicinal ingredients in Prazosin Hydrochloride drug includes Prazosin Hydrochloride - 1 mg/1 . The currest status of Prazosin Hydrochloride drug is Active.

Drug Information:

Drug NDC: 0378-1101
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name: Prazosin Hydrochloride
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type: Human Prescription Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name: Prazosin Hydrochloride
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: Mylan Pharmaceuticals Inc.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: Capsule
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status: Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:PRAZOSIN HYDROCHLORIDE - 1 mg/1
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:ORAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Marketing Category: ANDA
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (ANDA), BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
Marketing Start Date: 28 Feb, 1989
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 22 Dec, 2024
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
Application Number: ANDA072575
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
Listing Expiration Date: 31 Dec, 2023
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Manufacturer Name:Mylan Pharmaceuticals Inc.
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
RxCUI:198141
312593
312594
The RxNorm Concept Unique Identifier. RxCUI is a unique number that describes a semantic concept about the drug product, including its ingredients, strength, and dose forms.
Original Packager:Yes
Whether or not the drug has been repackaged for distribution.
UPC:0303783205014
0303782302011
0303781101011
UPC stands for Universal Product Code.
UNII:X0Z7454B90
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.
Pharmacologic Class:Adrenergic alpha-Antagonists [MoA]
alpha-Adrenergic Blocker [EPC]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDCDescriptionMarketing Start DateMarketing End DateSample Available
0378-1101-01100 CAPSULE in 1 BOTTLE, PLASTIC (0378-1101-01)28 Feb, 1989N/ANo
0378-1101-101000 CAPSULE in 1 BOTTLE, PLASTIC (0378-1101-10)28 Feb, 1989N/ANo
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Product Elements:

Prazosin hydrochloride prazosin hydrochloride prazosin hydrochloride prazosin silicon dioxide lactose monohydrate magnesium stearate microcrystalline cellulose ferrosoferric oxide gelatin, unspecified ferric oxide red titanium dioxide ferric oxide yellow d&c yellow no. 10 fd&c green no. 3 ammonia propylene glycol shellac dimethicone dark green opaque light brown opaque mylan;1101 prazosin hydrochloride prazosin hydrochloride prazosin hydrochloride prazosin silicon dioxide lactose monohydrate magnesium stearate microcrystalline cellulose ferrosoferric oxide gelatin, unspecified ferric oxide red titanium dioxide ferric oxide yellow d&c red no. 28 d&c yellow no. 10 fd&c blue no. 1 fd&c red no. 40 ammonia propylene glycol shellac dimethicone brown opaque light brown opaque mylan;2302 prazosin hydrochloride prazosin hydrochloride prazosin hydrochloride prazosin silicon dioxide lactose monohydrate magnesium stearate microcrystalline cellulose ferrosoferric oxide gelatin, unspecified ferric oxide red titanium dioxide ferric oxide yellow fd&c blue no. 1 ammonia propylene glycol shellac dimethicone light blue opaque light brown opaque mylan;3205

Drug Interactions:

Interactions drug interactions prazosin hydrochloride capsules have been administered without any adverse drug interaction in limited clinical experience to date with the following: (1) cardiac glycosides?digitalis and digoxin; (2) hypoglycemics?insulin, chlorpropamide, phenformin, tolazamide, and tolbutamide; (3) tranquilizers and sedatives?chlordiazepoxide, diazepam, and phenobarbital; (4) antigout?allopurinol, colchicine, and probenecid; (5) antiarrhythmics?procainamide, propranolol (see warnings however), and quinidine; and (6) analgesics, antipyretics and anti-inflammatories-propoxyphene, aspirin, indomethacin, and phenylbutazone. addition of a diuretic or other antihypertensive agent to prazosin hydrochloride capsules have been shown to cause an additive hypotensive effect. this effect can be minimized by reducing the prazosin hydrochloride capsules dose to 1 to 2 mg three times a day, by introducing additional antihypertensive drugs cautiously, and then by retitrating prazosin h
ydrochloride capsules based on clinical response. concomitant administration of prazosin hydrochloride capsules with a phosphodiesterase-5 (pde-5) inhibitor can result in additive blood pressure lowering effects and symptomatic hypotension (see dosage and administration ). drug/laboratory test interactions in a study on five patients given from 12 to 24 mg of prazosin per day for 10 to 14 days, there was an average increase of 42% in the urinary metabolite of norepinephrine and an average increase in urinary vma of 17%. therefore, false positive results may occur in screening tests for pheochromocytoma in patients who are being treated with prazosin. if an elevated vma is found, prazosin should be discontinued and the patient retested after a month.

Drug interactions prazosin hydrochloride capsules have been administered without any adverse drug interaction in limited clinical experience to date with the following: (1) cardiac glycosides?digitalis and digoxin; (2) hypoglycemics?insulin, chlorpropamide, phenformin, tolazamide, and tolbutamide; (3) tranquilizers and sedatives?chlordiazepoxide, diazepam, and phenobarbital; (4) antigout?allopurinol, colchicine, and probenecid; (5) antiarrhythmics?procainamide, propranolol (see warnings however), and quinidine; and (6) analgesics, antipyretics and anti-inflammatories-propoxyphene, aspirin, indomethacin, and phenylbutazone. addition of a diuretic or other antihypertensive agent to prazosin hydrochloride capsules have been shown to cause an additive hypotensive effect. this effect can be minimized by reducing the prazosin hydrochloride capsules dose to 1 to 2 mg three times a day, by introducing additional antihypertensive drugs cautiously, and then by retitrating prazosin hydrochloride
capsules based on clinical response. concomitant administration of prazosin hydrochloride capsules with a phosphodiesterase-5 (pde-5) inhibitor can result in additive blood pressure lowering effects and symptomatic hypotension (see dosage and administration ).

Indications and Usage:

Indications and usage prazosin hydrochloride capsules are indicated for the treatment of hypertension, to lower blood pressure. lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. these benefits have been seen in controlled trials of antihypertensive drugs from a wide variety of pharmacologic classes, including this drug. control of high blood pressure should be part of comprehensive cardiovascular risk management, including, as appropriate, lipid control, diabetes management, antithrombotic therapy, smoking cessation, exercise, and limited sodium intake. many patients will require more than one drug to achieve blood pressure goals. for specific advice on goals and management, see published guidelines, such as those of the national high blood pressure education program’s joint national committee on prevention, detection, evaluation, and treatment of high blood pressure (jnc). numerous antihypertensive drug
s, from a variety of pharmacologic classes and with different mechanisms of action, have been shown in randomized controlled trials to reduce cardiovascular morbidity and mortality, and it can be concluded that it is blood pressure reduction, and not some other pharmacologic property of the drugs, that is largely responsible for those benefits. the largest and most consistent cardiovascular outcome benefit has been a reduction in the risk of stroke, but reductions in myocardial infarction and cardiovascular mortality also have been seen regularly. elevated systolic or diastolic pressure causes increased cardiovascular risk, and the absolute risk increase per mmhg is greater at higher blood pressures, so that even modest reductions of severe hypertension can provide substantial benefit. relative risk reduction from blood pressure reduction is similar across populations with varying absolute risk, so the absolute benefit is greater in patients who are at higher risk independent of their hypertension (for example, patients with diabetes or hyperlipidemia), and such patients would be expected to benefit from more aggressive treatment to a lower blood pressure goal. some antihypertensive drugs have smaller blood pressure effects (as monotherapy) in black patients, and many antihypertensive drugs have additional approved indications and effects (e.g., on angina, heart failure, or diabetic kidney disease). these considerations may guide selection of therapy. prazosin hydrochloride capsules can be used alone or in combination with other antihypertensive drugs such as diuretics or beta-adrenergic blocking agents.

Warnings:

Warnings as with all alpha-blockers, prazosin hydrochloride capsules may cause syncope with sudden loss of consciousness. in most cases, this is believed to be due to an excessive postural hypotensive effect, although occasionally the syncopal episode has been preceded by a bout of severe tachycardia with heart rates of 120?160 beats per minute. syncopal episodes have usually occurred within 30 to 90 minutes of the initial dose of the drug; occasionally, they have been reported in association with rapid dosage increases or the introduction of another antihypertensive drug into the regimen of a patient taking high doses of prazosin hydrochloride capsules. the incidence of syncopal episodes is approximately 1% in patients given an initial dose of 2 mg or greater. clinical trials conducted during the investigational phase of this drug suggest that syncopal episodes can be minimized by limiting the initial dose of the drug to 1 mg, by subsequently increasing the dosage slowly, and by intro
ducing any additional antihypertensive drugs into the patient’s regimen with caution (see dosage and administration ). hypotension may develop in patients given prazosin hydrochloride capsules who are also receiving a beta-blocker such as propranolol. if syncope occurs, the patient should be placed in the recumbent position and treated supportively as necessary. this adverse effect is self-limiting and in most cases does not recur after the initial period of therapy or during subsequent dose titration. patients should always be started on the 1 mg capsules of prazosin hydrochloride capsules. the 2 and 5 mg capsules are not indicated for initial therapy. more common than loss of consciousness are the symptoms often associated with lowering of the blood pressure, namely, dizziness and lightheadedness. the patient should be cautioned about these possible adverse effects and advised what measures to take should they develop. the patient should also be cautioned to avoid situations where injury could result should syncope occur during the initiation of prazosin hydrochloride capsules therapy. priapism: prolonged erections and priapism have been reported with alpha-1 blockers including prazosin in post marketing experience. in the event of an erection that persists longer than 4 hours, seek immediate medical assistance. if priapism is not treated immediately, penile tissue damage and permanent loss of potency could result.

General Precautions:

General intraoperative floppy iris syndrome (ifis) has been observed during cataract surgery in some patients treated with alpha-1 blockers. this variant of small pupil syndrome is characterized by the combination of a flaccid iris that billows in response to intraoperative irrigation currents, progressive intraoperative miosis despite preoperative dilation with standard mydriatic drugs, and potential prolapse of the iris toward the phacoemulsification incisions. the patient’s ophthalmologist should be prepared for possible modifications to the surgical technique, such as the utilization of iris hooks, iris dilator rings, or viscoelastic substances. there does not appear to be a benefit of stopping alpha-1 blocker therapy prior to cataract surgery.

Dosage and Administration:

Dosage and administration the dose of prazosin hydrochloride capsules should be adjusted according to the patient’s individual blood pressure response. the following is a guide to its administration: initial dose: 1 mg two or three times a day (see warnings ). maintenance dose: dosage may be slowly increased to a total daily dose of 20 mg given in divided doses. the therapeutic dosages most commonly employed have ranged from 6 mg to 15 mg daily given in divided doses. doses higher than 20 mg usually do not increase efficacy, however a few patients may benefit from further increases up to a daily dose of 40 mg given in divided doses. after initial titration some patients can be maintained adequately on a twice daily dosage regimen. use with other drugs: when adding a diuretic or other antihypertensive agent, the dose of prazosin hydrochloride capsules should be reduced to 1 mg or 2 mg three times a day and retitration then carried out. concomitant administration of prazosin hydrochlori
de capsules with a pde-5 inhibitor can result in additive blood pressure lowering effects and symptomatic hypotension; therefore, pde-5 inhibitor therapy should be initiated at the lowest dose in patients taking prazosin hydrochloride capsules.

Contraindications:

Contraindications prazosin hydrochloride capsules are contraindicated in patients with known sensitivity to quinazolines, prazosin, or any of the inert ingredients.

Adverse Reactions:

Adverse reactions clinical trials were conducted on more than 900 patients. during these trials and subsequent marketing experience, the most frequent reactions associated with prazosin hydrochloride capsules therapy are: dizziness 10.3%, headache 7.8%, drowsiness 7.6%, lack of energy 6.9%, weakness 6.5%, palpitations 5.3%, and nausea 4.9%. in most instances, side effects have disappeared with continued therapy or have been tolerated with no decrease in dose of drug. less frequent adverse reactions which are reported to occur in 1?4% of patients are: gastrointestinal: vomiting, diarrhea, constipation. cardiovascular: edema, orthostatic hypotension, dyspnea, syncope. central nervous system: vertigo, depression, nervousness. dermatologic: rash. genitourinary: urinary frequency. eent: blurred vision, reddened sclera, epistaxis, dry mouth, nasal congestion. in addition, fewer than 1% of patients have reported the following (in some instances, exact causal relationships have not been establ
ished): gastrointestinal: abdominal discomfort and/or pain, liver function abnormalities, pancreatitis. cardiovascular: tachycardia. central nervous system: paresthesia, hallucinations. dermatologic: pruritus, alopecia, lichen planus. genitourinary: incontinence, impotence, priapism. eent: tinnitus. other: diaphoresis, fever, positive ana titer, arthralgia. single reports of pigmentary mottling and serous retinopathy, and a few reports of cataract development or disappearance have been reported. in these instances, the exact causal relationship has not been established because the baseline observations were frequently inadequate. in more specific slit-lamp and funduscopic studies, which included adequate baseline examinations, no drug-related abnormal ophthalmological findings have been reported. literature reports exist associating prazosin hydrochloride capsules therapy with a worsening of pre-existing narcolepsy. a causal relationship is uncertain in these cases. in post-marketing experience, the following adverse events have been reported: autonomic nervous system: flushing. body as a whole: allergic reaction, asthenia, malaise, pain. cardiovascular: general: angina pectoris, hypotension. endocrine: gynecomastia. heart rate/rhythm: bradycardia. psychiatric: insomnia. skin/appendages: urticaria. vascular (extracardiac): vasculitis. vision: eye pain. special senses: during cataract surgery, a variant of small pupil syndrome known as intraoperative floppy iris syndrome (ifis) has been reported in association with alpha-1 blocker therapy (see precautions ).

Drug Interactions:

Interactions drug interactions prazosin hydrochloride capsules have been administered without any adverse drug interaction in limited clinical experience to date with the following: (1) cardiac glycosides?digitalis and digoxin; (2) hypoglycemics?insulin, chlorpropamide, phenformin, tolazamide, and tolbutamide; (3) tranquilizers and sedatives?chlordiazepoxide, diazepam, and phenobarbital; (4) antigout?allopurinol, colchicine, and probenecid; (5) antiarrhythmics?procainamide, propranolol (see warnings however), and quinidine; and (6) analgesics, antipyretics and anti-inflammatories-propoxyphene, aspirin, indomethacin, and phenylbutazone. addition of a diuretic or other antihypertensive agent to prazosin hydrochloride capsules have been shown to cause an additive hypotensive effect. this effect can be minimized by reducing the prazosin hydrochloride capsules dose to 1 to 2 mg three times a day, by introducing additional antihypertensive drugs cautiously, and then by retitrating prazosin h
ydrochloride capsules based on clinical response. concomitant administration of prazosin hydrochloride capsules with a phosphodiesterase-5 (pde-5) inhibitor can result in additive blood pressure lowering effects and symptomatic hypotension (see dosage and administration ). drug/laboratory test interactions in a study on five patients given from 12 to 24 mg of prazosin per day for 10 to 14 days, there was an average increase of 42% in the urinary metabolite of norepinephrine and an average increase in urinary vma of 17%. therefore, false positive results may occur in screening tests for pheochromocytoma in patients who are being treated with prazosin. if an elevated vma is found, prazosin should be discontinued and the patient retested after a month.

Drug interactions prazosin hydrochloride capsules have been administered without any adverse drug interaction in limited clinical experience to date with the following: (1) cardiac glycosides?digitalis and digoxin; (2) hypoglycemics?insulin, chlorpropamide, phenformin, tolazamide, and tolbutamide; (3) tranquilizers and sedatives?chlordiazepoxide, diazepam, and phenobarbital; (4) antigout?allopurinol, colchicine, and probenecid; (5) antiarrhythmics?procainamide, propranolol (see warnings however), and quinidine; and (6) analgesics, antipyretics and anti-inflammatories-propoxyphene, aspirin, indomethacin, and phenylbutazone. addition of a diuretic or other antihypertensive agent to prazosin hydrochloride capsules have been shown to cause an additive hypotensive effect. this effect can be minimized by reducing the prazosin hydrochloride capsules dose to 1 to 2 mg three times a day, by introducing additional antihypertensive drugs cautiously, and then by retitrating prazosin hydrochloride
capsules based on clinical response. concomitant administration of prazosin hydrochloride capsules with a phosphodiesterase-5 (pde-5) inhibitor can result in additive blood pressure lowering effects and symptomatic hypotension (see dosage and administration ).

Use in Pregnancy:

Usage in pregnancy prazosin hydrochloride capsules has been shown to be associated with decreased litter size at birth, 1, 4, and 21 days of age in rats when given doses more than 225 times the usual maximum recommended human dose. no evidence of drug-related external, visceral, or skeletal fetal abnormalities were observed. no drug-related external, visceral, or skeletal abnormalities were observed in fetuses of pregnant rabbits and pregnant monkeys at doses more than 225 times and 12 times the usual maximum recommended human dose, respectively. the use of prazosin and a beta-blocker for the control of severe hypertension in 44 pregnant women revealed no drug-related fetal abnormalities or adverse effects. therapy with prazosin was continued for as long as 14 weeks. 1 prazosin has also been used alone or in combination with other hypotensive agents in severe hypertension of pregnancy by other investigators. no fetal or neonatal abnormalities have been reported with the use of prazosin
. 2 there are no adequate and well controlled studies which establish the safety of prazosin hydrochloride capsules in pregnant women. prazosin hydrochloride capsules should be used during pregnancy only if the potential benefit justifies the potential risk to the mother and fetus.

Pediatric Use:

Pediatric use safety and effectiveness in children have not been established.

Overdosage:

Overdosage accidental ingestion of at least 50 mg of prazosin hydrochloride capsules in a two year old child resulted in profound drowsiness and depressed reflexes. no decrease in blood pressure was noted. recovery was uneventful. should overdosage lead to hypotension, support of the cardiovascular system is of first importance. restoration of blood pressure and normalization of heart rate may be accomplished by keeping the patient in the supine position. if this measure is inadequate, shock should first be treated with volume expanders. if necessary, vasopressors should then be used. renal function should be monitored and supported as needed. laboratory data indicate prazosin hydrochloride capsules are not dialysable because it is protein bound.

Description:

Description prazosin hydrochloride capsules, usp a quinazoline derivative, is the first of a new chemical class of antihypertensives. it is the hydrochloride salt of 1-(4-amino-6,7-dimethoxy-2-quinazolinyl)-4-(2-furoyl) piperazine and its structural formula is: it is a white to tan powder, slightly soluble in water and methanol, very slightly soluble in alcohol, practically insoluble in chloroform and acetone and has a molecular weight of 419.87. each capsule, for oral use, contains prazosin hydrochloride, usp equivalent (as the polyhydrate) to 1 mg, 2 mg or 5 mg of prazosin. molecular formula c 19 h 21 n 5 o 4 • hcl inert ingredients in the formulations are: colloidal silicon dioxide, lactose monohydrate, magnesium stearate and microcrystalline cellulose. the empty gelatin capsules contain black iron oxide, gelatin, red iron oxide, titanium dioxide and yellow iron oxide. in addition, the 1 mg empty gelatin capsules contain d&c yellow no. 10 and fd&c green no. 3; the 2 mg empty gelatin capsules contain d&c red no. 28, d&c yellow no. 10, fd&c blue no. 1 and fd&c red no. 40; and the 5 mg empty gelatin capsules contain fd&c blue no. 1. the imprinting ink also contains ammonium hydroxide, propylene glycol, shellac glaze, simethicone and titanium dioxide. prazosin hcl molecular formula

Clinical Pharmacology:

Clinical pharmacology the exact mechanism of the hypotensive action of prazosin is unknown. prazosin causes a decrease in total peripheral resistance and was originally thought to have a direct relaxant action on vascular smooth muscle. recent animal studies, however, have suggested that the vasodilator effect of prazosin is also related to blockade of postsynaptic alpha-adrenoceptors. the results of dog forelimb experiments demonstrate that the peripheral vasodilator effect of prazosin is confined mainly to the level of the resistance vessels (arterioles). unlike conventional alpha-blockers, the antihypertensive action of prazosin is usually not accompanied by a reflex tachycardia. tolerance has not been observed to develop in long term therapy. hemodynamic studies have been carried out in man following acute single dose administration and during the course of long term maintenance therapy. the results confirm that the therapeutic effect is a fall in blood pressure unaccompanied by a
clinically significant change in cardiac output, heart rate, renal blood flow and glomerular filtration rate. there is no measurable negative chronotropic effect. in clinical studies to date, prazosin hydrochloride has not increased plasma renin activity. in man, blood pressure is lowered in both the supine and standing positions. this effect is most pronounced on the diastolic blood pressure. following oral administration, human plasma concentrations reach a peak at about three hours with a plasma half-life of two to three hours. the drug is highly bound to plasma protein. bioavailability studies have demonstrated that the total absorption relative to the drug in a 20% alcoholic solution is 90%, resulting in peak levels approximately 65% of that of the drug in solution. animal studies indicate that prazosin hydrochloride is extensively metabolized, primarily by demethylation and conjugation, and excreted mainly via bile and feces. less extensive human studies suggest similar metabolism and excretion in man. in clinical studies in which lipid profiles were followed, there were generally no adverse changes noted between pre- and post-treatment lipid levels.

Carcinogenesis and Mutagenesis and Impairment of Fertility:

Carcinogenesis, mutagenesis, impairment of fertility no carcinogenic potential was demonstrated in an 18 month study in rats with prazosin hydrochloride capsules at dose levels more than 225 times the usual maximum recommended human dose of 20 mg per day. prazosin hydrochloride capsules were not mutagenic in in vivo genetic toxicology studies. in a fertility and general reproductive performance study in rats, both males and females, treated with 75 mg/kg (225 times the usual maximum recommended human dose), demonstrated decreased fertility, while those treated with 25 mg/kg (75 times the usual maximum recommended human dose) did not. in chronic studies (one year or more) of prazosin hydrochloride capsules in rats and dogs, testicular changes consisting of atrophy and necrosis occurred at 25 mg/kg/day (75 times the usual maximum recommended human dose). no testicular changes were seen in rats or dogs at 10 mg/kg/day (30 times the usual maximum recommended human dose). in view of the tes
ticular changes observed in animals, 105 patients on long term prazosin hydrochloride capsules therapy were monitored for 17-ketosteroid excretion and no changes indicating a drug effect were observed. in addition, 27 males on prazosin hydrochloride capsules for up to 51 months did not have changes in sperm morphology suggestive of drug effect.

How Supplied:

How supplied prazosin hydrochloride capsules, usp are available containing prazosin hydrochloride, usp equivalent to 1 mg, 2 mg, or 5 mg of prazosin. the 1 mg capsules are hard-shell gelatin capsules with a dark green opaque cap and a light brown opaque body filled with a white to off-white powder blend. the capsule is axially printed with mylan over 1101 in white ink on both the cap and body. they are available as follows: ndc 0378-1101-01 bottles of 100 capsules ndc 0378-1101-10 bottles of 1000 capsules the 2 mg capsules are hard-shell gelatin capsules with a brown opaque cap and a light brown opaque body filled with a white to off-white powder blend. the capsule is axially printed with mylan over 2302 in white ink on both the cap and body. they are available as follows: ndc 0378-2302-01 bottles of 100 capsules ndc 0378-2302-10 bottles of 1000 capsules the 5 mg capsules are hard-shell gelatin capsules with a light blue opaque cap and a light brown opaque body filled with a white to o
ff-white powder blend. the capsule is axially printed with mylan over 3205 in white ink on both the cap and body. they are available as follows: ndc 0378-3205-01 bottles of 100 capsules ndc 0378-3205-25 bottles of 250 capsules store at 20° to 25°c (68° to 77°f). [see usp controlled room temperature.] protect from moisture and light. dispense in a tight, light-resistant container as defined by the usp using a child-resistant closure.

Information for Patients:

Information for patients dizziness or drowsiness may occur after the first dose of this medicine. avoid driving or performing hazardous tasks for the first 24 hours after taking this medicine or when the dose is increased. dizziness, lightheadedness, or fainting may occur, especially when rising from a lying or sitting position. getting up slowly may help lessen the problem. these effects may also occur if you drink alcohol, stand for long periods of time, exercise, or if the weather is hot. while taking prazosin hydrochloride capsules, be careful in the amount of alcohol you drink. also, use extra care during exercise or hot weather, or if standing for long periods. check with your physician if you have any questions.

Package Label Principal Display Panel:

Principal display panel – 1 mg ndc 0378-1101-01 prazosin hydrochloride capsules, usp 1 mg* rx only 100 capsules *each capsule contains prazosin hydrochloride, usp equivalent to 1 mg of prazosin. dispense in a tight, light-resistant container as defined in the usp using a child-resistant closure. keep container tightly closed. keep this and all medication out of the reach of children. store at 20° to 25°c (68° to 77°f). [see usp controlled room temperature.] protect from moisture and light. usual dosage: see accompanying prescribing information. manufactured for: mylan pharmaceuticals inc. morgantown, wv 26505 u.s.a. made in puerto rico mylan.com rvpl1101a prazosin hcl capsules, usp 1 mg

Principal display panel – 2 mg ndc 0378-2302-01 prazosin hydrochloride capsules, usp 2 mg* rx only 100 capsules *each capsule contains prazosin hydrochloride, usp equivalent to 2 mg of prazosin. dispense in a tight, light-resistant container as defined in the usp using a child-resistant closure. keep container tightly closed. keep this and all medication out of the reach of children. store at 20° to 25°c (68° to 77°f). [see usp controlled room temperature.] protect from moisture and light. usual dosage: see accompanying prescribing information. manufactured for: mylan pharmaceuticals inc. morgantown, wv 26505 u.s.a. made in puerto rico mylan.com rvpl2302a prazosin hcl capsules, usp 2 mg

Principal display panel – 5 mg ndc 0378-3205-01 prazosin hydrochloride capsules, usp 5 mg* rx only 100 capsules *each capsule contains prazosin hydrochloride, usp equivalent to 5 mg of prazosin. dispense in a tight, light-resistant container as defined in the usp using a child-resistant closure. keep container tightly closed. keep this and all medication out of the reach of children. store at 20° to 25°c (68° to 77°f). [see usp controlled room temperature.] protect from moisture and light. usual dosage: see accompanying prescribing information. manufactured for: mylan pharmaceuticals inc. morgantown, wv 26505 u.s.a. made in puerto rico mylan.com rvpl3205a prazosin hcl capsules, usp 5 mg


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