nifedipine - 55154-5357-0 - (nifedipine)

Alphabetical Index


Drug Information of nifedipine

Product NDC: 55154-5357
Proprietary Name: nifedipine
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 nifedipine

Product NDC: 55154-5357
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA019684
Marketing Category: ANDA
Start Marketing Date: 20070620

Package Information of nifedipine

Package NDC: 55154-5357-0
Package Description: 1 BLISTER PACK in 1 BAG (55154-5357-0) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of nifedipine

NDC Code 55154-5357-0
Proprietary Name nifedipine
Package Description 1 BLISTER PACK in 1 BAG (55154-5357-0) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 55154-5357
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name nifedipine
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20070620
Marketing Category Name ANDA
Labeler Name Cardinal Health
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