Nifedipine - 68788-0167-9 - (Nifedipine)

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Drug Information of Nifedipine

Product NDC: 68788-0167
Proprietary Name: Nifedipine
Non Proprietary Name: Nifedipine
Active Ingredient(s): 30    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: 68788-0167
Labeler Name: Preferred Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077127
Marketing Category: ANDA
Start Marketing Date: 20130319

Package Information of Nifedipine

Package NDC: 68788-0167-9
Package Description: 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-0167-9)

NDC Information of Nifedipine

NDC Code 68788-0167-9
Proprietary Name Nifedipine
Package Description 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-0167-9)
Product NDC 68788-0167
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nifedipine
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20130319
Marketing Category Name ANDA
Labeler Name Preferred 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 Nifedipine


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