Nifedipine - 49884-678-01 - (Nifedipine)

Alphabetical Index


Drug Information of Nifedipine

Product NDC: 49884-678
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: 49884-678
Labeler Name: Par Pharmaceutical, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077899
Marketing Category: ANDA
Start Marketing Date: 20070622

Package Information of Nifedipine

Package NDC: 49884-678-01
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (49884-678-01)

NDC Information of Nifedipine

NDC Code 49884-678-01
Proprietary Name Nifedipine
Package Description 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (49884-678-01)
Product NDC 49884-678
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nifedipine
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20070622
Marketing Category Name ANDA
Labeler Name Par Pharmaceutical, 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