Amiloride Hydrochloride


Windlas Biotech Limited
Human Prescription Drug
NDC 57721-671
Amiloride Hydrochloride is a human prescription drug labeled by 'Windlas Biotech Limited'. National Drug Code (NDC) number for Amiloride Hydrochloride is 57721-671. This drug is available in dosage form of Tablet. The names of the active, medicinal ingredients in Amiloride Hydrochloride drug includes Amiloride Hydrochloride - 5 mg/1 . The currest status of Amiloride Hydrochloride drug is Active.

Drug Information:

Drug NDC: 57721-671
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: Amiloride 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: Amiloride Hydrochloride
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: Windlas Biotech Limited
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: Tablet
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:AMILORIDE HYDROCHLORIDE - 5 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: 01 Dec, 2021
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 29 Dec, 2025
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: ANDA204180
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:WINDLAS BIOTECH LIMITED
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
RxCUI:977880
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.
UNII:FZJ37245UC
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:Decreased Renal K+ Excretion [PE]
Increased Diuresis [PE]
Potassium-sparing Diuretic [EPC]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDCDescriptionMarketing Start DateMarketing End DateSample Available
57721-671-01100 TABLET in 1 BOTTLE (57721-671-01)01 Dec, 2021N/ANo
57721-671-05500 TABLET in 1 BOTTLE (57721-671-05)01 Dec, 2021N/ANo
57721-671-0630 TABLET in 1 BOTTLE (57721-671-06)01 Dec, 2021N/ANo
57721-671-101000 TABLET in 1 BOTTLE (57721-671-10)01 Dec, 2021N/ANo
57721-671-1690 TABLET in 1 BOTTLE (57721-671-16)01 Dec, 2021N/ANo
57721-671-3010 BLISTER PACK in 1 CARTON (57721-671-30) / 10 TABLET in 1 BLISTER PACK01 Dec, 2021N/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:

Amiloride hydrochloride amiloride hydrochloride microcrystalline cellulose silicon dioxide croscarmellose sodium d&c yellow no. 10 dibasic calcium phosphate dihydrate fd&c yellow no. 6 magnesium stearate povidone k30 amiloride hydrochloride amiloride amiloride hydrochloride anhydrous 671

Drug Interactions:

Drug interactions when amiloride hydrochloride is administered concomitantly with an angiotensin-converting enzyme inhibitor, an angiotensin ii receptor antagonist, cyclosporine or tacrolimus, the risk of hyperkalemia may be increased. therefore, if concomitant use of these agents is indicated because of demonstrated hypokalemia, they should be used with caution and with frequent monitoring of serum potassium. (see warnings ). lithium generally should not be given with diuretics because they reduce its renal clearance and add a high risk of lithium toxicity. read circulars for lithium preparations before use of such concomitant therapy. in some patients, the administration of a non-steroidal anti-inflammatory agent can reduce the diuretic, natriuretic, and antihypertensive effects of loop, potassium-sparing and thiazide diuretics. therefore, when amiloride hydrochloride and non-steroidal anti-inflammatory agents are used concomitantly, the patient should be observed closely to determin
e if the desired effect of the diuretic is obtained. since indomethacin and potassium-sparing diuretics, including amiloride hydrochloride, may each be associated with increased serum potassium levels, the potential effects on potassium kinetics and renal function should be considered when these agents are administered concurrently.

Boxed Warning:

Hyperkalemia like other potassium-conserving agents, amiloride may cause hyperkalemia (serum potassium levels greater than 5.5 meq per liter) which, if uncorrected, is potentially fatal. hyperkalemia occurs commonly (about 10%) when amiloride is used without a kaliuretic diuretic. this incidence is greater in patients with renal impairment, diabetes mellitus (with or without recognized renal insufficiency), and in the elderly. when amiloride hydrochloride is used concomitantly with a thiazide diuretic in patients without these complications, the risk of hyperkalemia is reduced to about 1 to 2 percent. it is thus essential to monitor serum potassium levels carefully in any patient receiving amiloride, particularly when it is first introduced, at the time of diuretic dosage adjustments, and during any illness that could affect renal function.

Hyperkalemia like other potassium-conserving agents, amiloride may cause hyperkalemia (serum potassium levels greater than 5.5 meq per liter) which, if uncorrected, is potentially fatal. hyperkalemia occurs commonly (about 10%) when amiloride is used without a kaliuretic diuretic. this incidence is greater in patients with renal impairment, diabetes mellitus (with or without recognized renal insufficiency), and in the elderly. when amiloride hydrochloride is used concomitantly with a thiazide diuretic in patients without these complications, the risk of hyperkalemia is reduced to about 1 to 2 percent. it is thus essential to monitor serum potassium levels carefully in any patient receiving amiloride, particularly when it is first introduced, at the time of diuretic dosage adjustments, and during any illness that could affect renal function.

Indications and Usage:

Indications and usage amiloride hydrochloride tablets are indicated as adjunctive treatment with thiazide diuretics or other kaliuretic-diuretic agents in congestive heart failure or hypertension to: a. help restore normal serum potassium levels in patients who develop hypokalemia on the kaliuretic diuretic. b. prevent development of hypokalemia in patients who would be exposed to particular risk if hypokalemia were to develop, e.g., digitalized patients or patients with significant cardiac arrhythmias. the use of potassium-conserving agents is often unnecessary in patients receiving diuretics for uncomplicated essential hypertension when such patients have a normal diet. amiloride hydrochloride has little additive diuretic or antihypertensive effect when added to a thiazide diuretic. amiloride hydrochloride tablets should rarely be used alone. it has weak (compared with thiazides) diuretic and antihypertensive effects. used as single agents, potassium sparing diuretics, including amil
oride hydrochloride, result in an increased risk of hyperkalemia (approximately 10% with amiloride). amiloride hydrochloride tablets should be used alone only when persistent hypokalemia has been documented and only with careful titration of the dose and close monitoring of serum electrolytes.

Warnings:

Warnings

Dosage and Administration:

Dosage and administration amiloride hydrochloride should be administered with food. amiloride hydrochloride, one 5 mg tablet daily, should be added to the usual antihypertensive or diuretic dosage of a kaliuretic diuretic. the dosage may be increased to 10 mg per day, if necessary. more than two 5 mg tablets of amiloride hydrochloride daily usually are not needed, and there is little controlled experience with such doses. if persistent hypokalemia is documented with 10 mg, the dose can be increased to 15 mg, then 20 mg, with careful monitoring of electrolytes. in treating patients with congestive heart failure after an initial diuresis has been achieved, potassium loss may also decrease and the need for amiloride hydrochloride should be re-evaluated. dosage adjustment may be necessary. maintenance therapy may be on an intermittent basis. if it is necessary to use amiloride hydrochloride alone (see indications ), the starting dosage should be one 5 mg tablet daily. this dosage may be in
creased to 10 mg per day, if necessary. more than two 5 mg tablets usually are not needed, and there is little controlled experience with such doses. if persistent hypokalemia is documented with 10 mg, the dose can be increased to 15 mg, then 20 mg, with careful monitoring of electrolytes.

Contraindications:

Contraindications hyperkalemia amiloride hydrochloride tablets should not be used in the presence of elevated serum potassium levels (greater than 5.5 meq per liter). antikaliuretic therapy or potassium supplementation amiloride hydrochloride should not be given to patients receiving other potassium-conserving agents, such as spironolactone or triamterene. potassium supplementation in the form of medication, potassium-containing salt substitutes or a potassium-rich diet should not be used with amiloride hydrochloride except in severe and/or refractory cases of hypokalemia. such concomitant therapy can be associated with rapid increases in serum potassium levels. if potassium supplementation is used, careful monitoring of the serum potassium level is necessary. impaired renal function anuria, acute or chronic renal insufficiency, and evidence of diabetic nephropathy are contraindications to the use of amiloride hydrochloride. patients with evidence of renal functional impairment (blood urea nitrogen [bun] levels over 30 mg per 100 ml or serum creatinine levels over 1.5 mg per 100 ml) or diabetes mellitus should not receive the drug without careful, frequent and continuing monitoring of serum electrolytes, creatinine, and bun levels. potassium retention associated with the use of an antikaliuretic agent is accentuated in the presence of renal impairment and may result in the rapid development of hyperkalemia. hypersensitivity amiloride hydrochloride is contraindicated in patients who are hypersensitive to this product.

Hyperkalemia amiloride hydrochloride tablets should not be used in the presence of elevated serum potassium levels (greater than 5.5 meq per liter).

Antikaliuretic therapy or potassium supplementation amiloride hydrochloride should not be given to patients receiving other potassium-conserving agents, such as spironolactone or triamterene. potassium supplementation in the form of medication, potassium-containing salt substitutes or a potassium-rich diet should not be used with amiloride hydrochloride except in severe and/or refractory cases of hypokalemia. such concomitant therapy can be associated with rapid increases in serum potassium levels. if potassium supplementation is used, careful monitoring of the serum potassium level is necessary.

Impaired renal function anuria, acute or chronic renal insufficiency, and evidence of diabetic nephropathy are contraindications to the use of amiloride hydrochloride. patients with evidence of renal functional impairment (blood urea nitrogen [bun] levels over 30 mg per 100 ml or serum creatinine levels over 1.5 mg per 100 ml) or diabetes mellitus should not receive the drug without careful, frequent and continuing monitoring of serum electrolytes, creatinine, and bun levels. potassium retention associated with the use of an antikaliuretic agent is accentuated in the presence of renal impairment and may result in the rapid development of hyperkalemia.

Hypersensitivity amiloride hydrochloride is contraindicated in patients who are hypersensitive to this product.

Adverse Reactions:

Adverse reactions amiloride hydrochloride is usually well tolerated and, except for hyperkalemia (serum potassium levels greater than 5.5 meq per liter – see warnings ), significant adverse effects have been reported infrequently. minor adverse reactions were reported relatively frequently (about 20%) but the relationship of many of the reports to amiloride hydrochloride is uncertain and the overall frequency was similar in hydrochlorothiazide treated groups. nausea/anorexia, abdominal pain, flatulence, and mild skin rash have been reported and probably are related to amiloride. other adverse experiences that have been reported with amiloride are generally those known to be associated with diuresis, or with the underlying disease being treated. the adverse reactions for amiloride hydrochloride listed in the following table have been arranged into two groups: (1) incidence greater than one percent; and (2) incidence one percent or less. the incidence for group (1) was determined fr
om clinical studies conducted in the united states (837 patients treated with amiloride hydrochloride). the adverse effects listed in group (2) include reports from the same clinical studies and voluntary reports since marketing. the probability of a causal relationship exists between amiloride hydrochloride and these adverse reactions, some of which have been reported only rarely. incidence > 1% incidence ≤ 1% body as a whole headache* back pain weakness chest pain fatigability neck/shoulder ache pain, extremities cardiovascular none angina pectoris orthostatic hypotension arrhythmia palpitation digestive nausea/anorexia* jaundice diarrhea* gi bleeding vomiting* abdominal fullness abdominal pain gi disturbance gas pain thirst appetite changes heartburn constipation flatulence dyspepsia metabolic elevated serum potassium levels (>5.5 meq per liter)** none skin none skin rash itching dryness of mouth pruritus alopecia musculoskeletal muscle cramps joint pain leg ache nervous dizziness paresthesia encephalopathy tremors vertigo psychiatric none nervousness mental confusion insomnia decreased libido depression somnolence respiratory cough shortness of breath dyspnea special senses none visual disturbances nasal congestion tinnitus increased intraocular pressure urogenital impotence polyuria dysuria urinary frequency bladder spasms gynecomastia *reactions occurring in 3% to 8% of patients treated with amiloride hydrochloride. (those reactions occurring in less than 3% of the patients are unmarked.) **see warnings . causal relationship unknown other reactions have been reported but occurred under circumstances where a causal relationship could not be established. however, in these rarely reported events, that possibility cannot be excluded. therefore, these observations are listed to serve as alerting information to physicians. activation of probable pre-existing peptic ulcer aplastic anemia neutropenia abnormal liver function

Adverse Reactions Table:

Incidence > 1% Incidence 1%
Body as a Whole
Headache*Back pain
WeaknessChest pain
FatigabilityNeck/shoulder ache
Pain, extremities
Cardiovascular
NoneAngina pectoris
Orthostatic hypotension
Arrhythmia
Palpitation
Digestive
Nausea/anorexia*Jaundice
Diarrhea*GI bleeding
Vomiting*Abdominal fullness
Abdominal painGI disturbance
Gas painThirst
Appetite changesHeartburn
ConstipationFlatulence
Dyspepsia
Metabolic Elevated serum potassium levels (>5.5 mEq per liter)** None
Skin
NoneSkin rash
Itching
Dryness of mouth
Pruritus
Alopecia
Musculoskeletal
Muscle crampsJoint pain
Leg ache
Nervous
DizzinessParesthesia
EncephalopathyTremors
Vertigo
Psychiatric
NoneNervousness
Mental confusion
Insomnia
Decreased libido
Depression
Somnolence
Respiratory
CoughShortness of Breath
Dyspnea
Special Senses
NoneVisual disturbances
Nasal congestion
Tinnitus
Increased intraocular pressure
Urogenital
ImpotencePolyuria
Dysuria
Urinary frequency
Bladder spasms
Gynecomastia
*Reactions occurring in 3% to 8% of patients treated with amiloride hydrochloride.(Those reactions occurring in less than 3% of the patients are unmarked.)**See WARNINGS.

Drug Interactions:

Drug interactions when amiloride hydrochloride is administered concomitantly with an angiotensin-converting enzyme inhibitor, an angiotensin ii receptor antagonist, cyclosporine or tacrolimus, the risk of hyperkalemia may be increased. therefore, if concomitant use of these agents is indicated because of demonstrated hypokalemia, they should be used with caution and with frequent monitoring of serum potassium. (see warnings ). lithium generally should not be given with diuretics because they reduce its renal clearance and add a high risk of lithium toxicity. read circulars for lithium preparations before use of such concomitant therapy. in some patients, the administration of a non-steroidal anti-inflammatory agent can reduce the diuretic, natriuretic, and antihypertensive effects of loop, potassium-sparing and thiazide diuretics. therefore, when amiloride hydrochloride and non-steroidal anti-inflammatory agents are used concomitantly, the patient should be observed closely to determin
e if the desired effect of the diuretic is obtained. since indomethacin and potassium-sparing diuretics, including amiloride hydrochloride, may each be associated with increased serum potassium levels, the potential effects on potassium kinetics and renal function should be considered when these agents are administered concurrently.

Use in Pregnancy:

Pregnancy pregnancy category b. teratogenicity studies with amiloride hydrochloride in rabbits and mice given 20 and 25 times the maximum human dose, respectively, revealed no evidence of harm to the fetus, although studies showed that the drug crossed the placenta in modest amounts. reproduction studies in rats at 20 times the expected maximum daily dose for humans showed no evidence of impaired fertility. at approximately 5 or more times the expected maximum daily dose for humans, some toxicity was seen in adult rats and rabbits and a decrease in rat pup growth and survival occurred. there are, however, no adequate and well-controlled studies in pregnant women. because animal reproduction studies are not always predictive of human response, this drug should be used during pregnancy only if clearly needed.

Pediatric Use:

Pediatric use safety and effectiveness in pediatric patients have not been established.

Geriatric Use:

Geriatric use clinical studies of amiloride hydrochloride did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. other reported clinical experience has not identified differences in responses between the elderly and younger patients. in general, dose selection for an elderly patient should be cautious, usually starting at the low end of the dosing range, reflecting the greater frequency of decreased hepatic, renal or cardiac function, and of concomitant disease or other drug therapy. this drug is known to be substantially excreted by the kidney, and the risk of toxic reactions to this drug may be greater in patients with impaired renal function. because elderly patients are more likely to have decreased renal function, care should be taken in dose selection, and it may be useful to monitor renal function. (see contraindications, impaired renal function .)

Overdosage:

Overdosage no data are available in regard to overdosage in humans. the oral ld 50 of amiloride hydrochloride (calculated as the base) is 56 mg/kg in mice and 36 to 85 mg/kg in rats, depending on the strain. it is not known whether the drug is dialyzable. the most likely signs and symptoms to be expected with overdosage are dehydration and electrolyte imbalance. these can be treated by established procedures. therapy with amiloride hydrochloride should be discontinued and the patient observed closely. there is no specific antidote. emesis should be induced or gastric lavage performed. treatment is symptomatic and supportive. if hyperkalemia occurs, active measures should be taken to reduce the serum potassium levels.

Description:

Description amiloride hydrochloride, an antikaliuretic-diuretic agent, is a pyrazine-carbonyl-guanidine that is unrelated chemically to other known antikaliuretic or diuretic agents. it is the salt of a moderately strong base (pka 8.7). it is designated chemically as 3,5-diamino-6-chloro-n-(diaminomethylene) pyrazinecarboxamide monohydrochloride, dihydrate and has a molecular weight of 302.12. its molecular formula is c 6 h 8 cin 7 o•hcl•2h 2 o and its structural formula is: amiloride hydrochloride is a pale-yellow to greenish-yellow powder. it is freely soluble in dimethylsulphoxide; slightly soluble in water, ethyl alcohol and isopropyl alcohol; sparingly soluble in methyl alcohol; practically insoluble in acetone, chloroform, diethyl ether and ethyl acetate. each amiloride hydrochloride tablet intended for oral administration contains 5 mg of amiloride hydrochloride, calculated on the anhydrous basis. in addition, each tablet contains the following inactive ingredients: colloidal silicon dioxide, croscarmellose sodium, d&c yellow #10 aluminum lake, dibasic calcium phosphate dihydrate, fd & c yellow #6 aluminum lake, magnesium stearate, microcrystalline cellulose and povidone. structure

Clinical Pharmacology:

Clinical pharmacology amiloride hydrochloride is a potassium-conserving (antikaliuretic) drug that possesses weak (compared with thiazide diuretics) natriuretic, diuretic, and antihypertensive activity. these effects have been partially additive to the effects of thiazide diuretics in some clinical studies. when administered with a thiazide or loop diuretic, amiloride hydrochloride has been shown to decrease the enhanced urinary excretion of magnesium which occurs when a thiazide or loop diuretic is used alone. amiloride hydrochloride has potassium-conserving activity in patients receiving kaliuretic-diuretic agents. amiloride hydrochloride is not an aldosterone antagonist and its effects are seen even in the absence of aldosterone. amiloride hydrochloride exerts its potassium sparing effect through the inhibition of sodium reabsorption at the distal convoluted tubule, cortical collecting tubule and collecting duct; this decreases the net negative potential of the tubular lumen and red
uces both potassium and hydrogen secretion and their subsequent excretion. this mechanism accounts in large part for the potassium sparing action of amiloride. amiloride hydrochloride usually begins to act within 2 hours after an oral dose. its effect on electrolyte excretion reaches a peak between 6 and 10 hours and lasts about 24 hours. peak plasma levels are obtained in 3 to 4 hours and the plasma half-life varies from 6 to 9 hours. effects on electrolytes increase with single doses of amiloride hydrochloride up to approximately 15 mg. amiloride hydrochloride is not metabolized by the liver but is excreted unchanged by the kidneys. about 50 percent of a 20 mg dose of amiloride hydrochloride is excreted in the urine and 40 percent in the stool within 72 hours. amiloride hydrochloride has little effect on glomerular filtration rate or renal blood flow. because amiloride hydrochloride is not metabolized by the liver, drug accumulation is not anticipated in patients with hepatic dysfunction, but accumulation can occur if the hepatorenal syndrome develops.

Carcinogenesis and Mutagenesis and Impairment of Fertility:

Carcinogenesis, mutagenesis, impairment of fertility there was no evidence of a tumorigenic effect when amiloride hydrochloride was administered for 92 weeks to mice at doses up to 10 mg/kg/day (25 times the maximum daily human dose). amiloride hydrochloride has also been administered for 104 weeks to male and female rats at doses up to 6 and 8 mg/kg/day (15 and 20 times the maximum daily dose for humans, respectively) and showed no evidence of carcinogenicity. amiloride hydrochloride was devoid of mutagenic activity in various strains of salmonella typhimurium with or without a mammalian liver microsomal activation system (ames test).

How Supplied:

How supplied amiloride hydrochloride tablets usp, 5 mg are yellow colored, may be spotted, round shaped, biconvex, uncoated tablets, debossed with "671" on one side and plain on the other side and are supplied as follows: ndc 57721-671-06 in bottle of 30 tablets ndc 57721-671-16 in bottle of 90 tablets ndc 57721-671-01 in bottle of 100 tablets ndc 57721-671-05 in bottle of 500 tablets ndc 57721-671-10 in bottle of 1000 tablets ndc 57721-671-30 in unit-dose blister cartons of 100 (10 x 10) unit-dose tablets storage store at 20° to 25°c (68° to 77°f) [see usp controlled room temperature]. dispense in a tight container (usp). call your doctor for medical advice about side effects. you may report side effects to fda at 1-800-fda-1088. manufactured by: cadila healthcare ltd. baddi, india distributed by: windlas inc. 325 sharon park drive pmb # 202 menlo park, ca 94025 rev.: 12/17

Package Label Principal Display Panel:

Package label.principal display panel ndc 57721-671-01 in bottle of 100 tablets amiloride hydrochloride tablets, usp 5 mg rx only 100 tablets windlas healthcare pvt. ltd. bottle-label


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