Nifedipine - 52125-398-20 - (Nifedipine)

Alphabetical Index


Drug Information of Nifedipine

Product NDC: 52125-398
Proprietary Name: Nifedipine
Non Proprietary Name: Nifedipine
Active Ingredient(s): 90    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: 52125-398
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077410
Marketing Category: ANDA
Start Marketing Date: 20130514

Package Information of Nifedipine

Package NDC: 52125-398-20
Package Description: 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 VIAL (52125-398-20)

NDC Information of Nifedipine

NDC Code 52125-398-20
Proprietary Name Nifedipine
Package Description 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 VIAL (52125-398-20)
Product NDC 52125-398
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nifedipine
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20130514
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name NIFEDIPINE
Strength Number 90
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient]

Complete Information of Nifedipine


General Information