Nifedipine - 62175-262-32 - (Nifedipine)

Alphabetical Index


Drug Information of Nifedipine

Product NDC: 62175-262
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: 62175-262
Labeler Name: Kremers Urban Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077410
Marketing Category: ANDA
Start Marketing Date: 20071003

Package Information of Nifedipine

Package NDC: 62175-262-32
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-262-32)

NDC Information of Nifedipine

NDC Code 62175-262-32
Proprietary Name Nifedipine
Package Description 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-262-32)
Product NDC 62175-262
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nifedipine
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20071003
Marketing Category Name ANDA
Labeler Name Kremers Urban Pharmaceuticals 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