Adalat CC - 50419-701-05 - (nifedipine)

Alphabetical Index


Drug Information of Adalat CC

Product NDC: 50419-701
Proprietary Name: Adalat CC
Non Proprietary Name: nifedipine
Active Ingredient(s): 30    mg/1 & nbsp;   nifedipine
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Adalat CC

Product NDC: 50419-701
Labeler Name: Bayer HealthCare Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020198
Marketing Category: NDA
Start Marketing Date: 19930421

Package Information of Adalat CC

Package NDC: 50419-701-05
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50419-701-05)

NDC Information of Adalat CC

NDC Code 50419-701-05
Proprietary Name Adalat CC
Package Description 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50419-701-05)
Product NDC 50419-701
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name nifedipine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19930421
Marketing Category Name NDA
Labeler Name Bayer HealthCare Pharmaceuticals Inc.
Substance Name NIFEDIPINE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient]

Complete Information of Adalat CC


General Information