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Alfuzosin Hydrochloride - 60505-2850-0 - (Alfuzosin Hydrochloride)

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Drug Information of Alfuzosin Hydrochloride

Product NDC: 60505-2850
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: 60505-2850
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079013
Marketing Category: ANDA
Start Marketing Date: 20110718

Package Information of Alfuzosin Hydrochloride

Package NDC: 60505-2850-0
Package Description: 10 BLISTER PACK in 1 CARTON (60505-2850-0) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of Alfuzosin Hydrochloride

NDC Code 60505-2850-0
Proprietary Name Alfuzosin Hydrochloride
Package Description 10 BLISTER PACK in 1 CARTON (60505-2850-0) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 60505-2850
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Alfuzosin Hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110718
Marketing Category Name ANDA
Labeler Name Apotex Corp.
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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