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Alfuzosin Hydrochloride - 47335-956-08 - (Alfuzosin Hydrochloride)

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Drug Information of Alfuzosin Hydrochloride

Product NDC: 47335-956
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, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Alfuzosin Hydrochloride

Product NDC: 47335-956
Labeler Name: Sun Pharma Global FZE
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079057
Marketing Category: ANDA
Start Marketing Date: 20111122

Package Information of Alfuzosin Hydrochloride

Package NDC: 47335-956-08
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-08)

NDC Information of Alfuzosin Hydrochloride

NDC Code 47335-956-08
Proprietary Name Alfuzosin Hydrochloride
Package Description 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-08)
Product NDC 47335-956
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Alfuzosin Hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20111122
Marketing Category Name ANDA
Labeler Name Sun Pharma Global FZE
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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