Nifedipine - 54868-4531-3 - (Nifedipine)

Alphabetical Index


Drug Information of Nifedipine

Product NDC: 54868-4531
Proprietary Name: Nifedipine
Non Proprietary Name: Nifedipine
Active Ingredient(s): 60    mg/1 & nbsp;   Nifedipine
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Nifedipine

Product NDC: 54868-4531
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077899
Marketing Category: ANDA
Start Marketing Date: 20090305

Package Information of Nifedipine

Package NDC: 54868-4531-3
Package Description: 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (54868-4531-3)

NDC Information of Nifedipine

NDC Code 54868-4531-3
Proprietary Name Nifedipine
Package Description 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (54868-4531-3)
Product NDC 54868-4531
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nifedipine
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20090305
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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 Nifedipine


General Information