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Alfuzosin Hydrochloride - 64679-738-02 - (Alfuzosin Hydrochloride)

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Drug Information of Alfuzosin Hydrochloride

Product NDC: 64679-738
Proprietary Name: Alfuzosin Hydrochloride
Non Proprietary Name: Alfuzosin Hydrochloride
Active Ingredient(s): 10    mg/1 & nbsp;   Alfuzosin Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Alfuzosin Hydrochloride

Product NDC: 64679-738
Labeler Name: Wockhardt USA LLC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090221
Marketing Category: ANDA
Start Marketing Date: 20120815

Package Information of Alfuzosin Hydrochloride

Package NDC: 64679-738-02
Package Description: 100 TABLET in 1 BOTTLE (64679-738-02)

NDC Information of Alfuzosin Hydrochloride

NDC Code 64679-738-02
Proprietary Name Alfuzosin Hydrochloride
Package Description 100 TABLET in 1 BOTTLE (64679-738-02)
Product NDC 64679-738
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Alfuzosin Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120815
Marketing Category Name ANDA
Labeler Name Wockhardt USA LLC.
Substance Name ALFUZOSIN HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC]

Complete Information of Alfuzosin Hydrochloride


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