Afeditab - 0591-3194-01 - (Nifedipine)

Alphabetical Index


Drug Information of Afeditab

Product NDC: 0591-3194
Proprietary Name: Afeditab
Non Proprietary Name: Nifedipine
Active Ingredient(s): 60    mg/1 & nbsp;   Nifedipine
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Afeditab

Product NDC: 0591-3194
Labeler Name: Watson Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075659
Marketing Category: ANDA
Start Marketing Date: 20021101

Package Information of Afeditab

Package NDC: 0591-3194-01
Package Description: 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0591-3194-01)

NDC Information of Afeditab

NDC Code 0591-3194-01
Proprietary Name Afeditab
Package Description 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0591-3194-01)
Product NDC 0591-3194
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nifedipine
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20021101
Marketing Category Name ANDA
Labeler Name Watson Laboratories, Inc.
Substance Name NIFEDIPINE
Strength Number 60
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient]

Complete Information of Afeditab


General Information