Home > National Drug Code (NDC) > Alfuzosin Hydrochloride

Alfuzosin Hydrochloride - 31722-302-30 - (Alfuzosin Hydrochloride)

Alphabetical Index


Drug Information of Alfuzosin Hydrochloride

Product NDC: 31722-302
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: 31722-302
Labeler Name: Camber Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090284
Marketing Category: ANDA
Start Marketing Date: 20120118

Package Information of Alfuzosin Hydrochloride

Package NDC: 31722-302-30
Package Description: 24 BOTTLE in 1 CASE (31722-302-30) > 30 TABLET in 1 BOTTLE

NDC Information of Alfuzosin Hydrochloride

NDC Code 31722-302-30
Proprietary Name Alfuzosin Hydrochloride
Package Description 24 BOTTLE in 1 CASE (31722-302-30) > 30 TABLET in 1 BOTTLE
Product NDC 31722-302
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Alfuzosin Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120118
Marketing Category Name ANDA
Labeler Name Camber Pharmaceuticals
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


General Information