Nifedipine - 68788-9885-3 - (nifedipine)

Alphabetical Index


Drug Information of Nifedipine

Product NDC: 68788-9885
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: 68788-9885
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090649
Marketing Category: ANDA
Start Marketing Date: 20120214

Package Information of Nifedipine

Package NDC: 68788-9885-3
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-9885-3)

NDC Information of Nifedipine

NDC Code 68788-9885-3
Proprietary Name Nifedipine
Package Description 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-9885-3)
Product NDC 68788-9885
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name nifedipine
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120214
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, 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