Phenoxybenzamine Hydrochloride
Hikma Pharmaceuticals Usa Inc.
Human Prescription Drug
NDC 0054-0349Phenoxybenzamine Hydrochloride is a human prescription drug labeled by 'Hikma Pharmaceuticals Usa Inc.'. National Drug Code (NDC) number for Phenoxybenzamine Hydrochloride is 0054-0349. This drug is available in dosage form of Capsule. The names of the active, medicinal ingredients in Phenoxybenzamine Hydrochloride drug includes Phenoxybenzamine Hydrochloride - 10 mg/1 . The currest status of Phenoxybenzamine Hydrochloride drug is Active.
Drug Information:
| Drug NDC: | 0054-0349 |
| 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: | Phenoxybenzamine 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: | Phenoxybenzamine Hydrochloride |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Hikma Pharmaceuticals Usa 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: | PHENOXYBENZAMINE HYDROCHLORIDE - 10 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: | 10 Aug, 2015 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 18 Jan, 2026 |
| 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: | ANDA201050 |
| 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: | Hikma Pharmaceuticals USA Inc.
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| RxCUI: | 861402
|
| 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: | 0300540349257
|
| UPC stands for Universal Product Code. |
| UNII: | X1IEG24OHL
|
| 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 NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|
| 0054-0349-25 | 100 CAPSULE in 1 BOTTLE (0054-0349-25) | 10 Aug, 2015 | N/A | No |
| 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:
Phenoxybenzamine hydrochloride phenoxybenzamine hydrochloride phenoxybenzamine hydrochloride phenoxybenzamine anhydrous lactose fd&c red no. 40 gelatin, unspecified water sodium lauryl sulfate titanium dioxide shellac silicon dioxide ammonia ferrosoferric oxide isopropyl alcohol butyl alcohol propylene glycol 54;036
Indications and Usage:
Indications and usage phenoxybenzamine hydrochloride capsules are indicated in the treatment of pheochromocytoma, to control episodes of hypertension and sweating. if tachycardia is excessive, it may be necessary to use a beta -blocking agent concomitantly.
Warnings:
Warnings phenoxybenzamine-induced alpha -adrenergic blockade leaves beta -adrenergic receptors unopposed. compounds that stimulate both types of receptors may, therefore, produce an exaggerated hypotensive response and tachycardia.
General Precautions:
General administer with caution in patients with marked cerebral or coronary arteriosclerosis or renal damage. adrenergic blocking effect may aggravate symptoms of respiratory infections.
Dosage and Administration:
Dosage and administration the dosage should be adjusted to fit the needs of each patient. small initial doses should be slowly increased until the desired effect is obtained or the side effects from blockade become troublesome. after each increase, the patient should be observed on that level before instituting another increase . the dosage should be carried to a point where symptomatic relief and/or objective improvement are obtained, but not so high that the side effects from blockade become troublesome. initially, 10 mg of phenoxybenzamine hydrochloride twice a day. dosage should be increased every other day, usually to 20 to 40 mg 2 or 3 times a day, until an optimal dosage is obtained, as judged by blood pressure control. long-term use of phenoxybenzamine is not recommended (see precautions : carcinogenesis and mutagenesis ).
Contraindications:
Contraindications conditions where a fall in blood pressure may be undesirable; hypersensitivity to the drug or any of its components.
Adverse Reactions:
Adverse reactions the following adverse reactions have been observed, but there are insufficient data to support an estimate of their frequency. autonomic nervous system*: postural hypotension, tachycardia, inhibition of ejaculation, nasal congestion, miosis. *these so-called âside effectsâ are actually evidence of adrenergic blockade and vary according to the degree of blockade. miscellaneous: gastrointestinal irritation, drowsiness, fatigue.
Use in Pregnancy:
Pregnancy teratogenic effects: pregnancy category c: adequate reproductive studies in animals have not been performed with phenoxybenzamine hydrochloride. it is also not known whether phenoxybenzamine can cause fetal harm when administered to a pregnant woman. phenoxybenzamine should be given to a pregnant woman only if clearly needed.
Pediatric Use:
Pediatric use
Overdosage:
Overdosage symptoms - these are largely the result of blocking of the sympathetic nervous system and of the circulating epinephrine. they may include postural hypotension, resulting in dizziness or fainting; tachycardia, particularly postural; vomiting; lethargy; shock.
Description:
Description each phenoxybenzamine hydrochloride capsule, usp contains 10 mg of phenoxybenzamine hydrochloride, usp. inactive ingredients consist of anhydrous lactose, black monogramming ink, colloidal silicon dioxide and sodium lauryl sulfate. the black monogramming ink contains ammonium hydroxide, iron oxide black, isopropyl alcohol, n-butyl alcohol, propylene glycol, and shellac. the capsule shells also contain fd&c red no. 40, gelatin, purified water and titanium dioxide. phenoxybenzamine is n -(2-chloroethyl)- n -(1-methyl-2-phenoxyethyl)benzylamine hydrochloride: phenoxybenzamine hydrochloride is a white to almost white powder with a molecular weight of 340.3, which melts between 136° and 141°c. it is soluble in alcohol and chloroform; insoluble in ether and water. chem
Clinical Pharmacology:
Clinical pharmacology phenoxybenzamine hydrochloride is a long-acting, adrenergic, alpha -receptor blocking agent, which can produce and maintain âchemical sympathectomyâ by oral administration. it increases blood flow to the skin, mucosa and abdominal viscera, and lowers both supine and erect blood pressures. it has no effect on the parasympathetic system. twenty to 30 percent of orally administered phenoxybenzamine appears to be absorbed in the active form. 1 the half-life of orally administered phenoxybenzamine hydrochloride is not known; however, the half-life of intravenously administered drug is approximately 24 hours. demonstrable effects with intravenous administration persist for at least 3 to 4 days, and the effects of daily administration are cumulative for nearly a week. 1
How Supplied:
How supplied phenoxybenzamine hydrochloride capsules, usp 10 mg capsule is supplied as a red opaque/red opaque capsule with â54 036â printed in black on the cap and â54 036â printed in black ink on the capsule body, containing a white to off-white powder. ndc 0054-0349-25: bottle of 100 capsules storage store at 20° to 25°c (68° to 77°f). [see usp controlled room temperature.]
Package Label Principal Display Panel:
Package/label display panel bottle1