Nifedipine - 54868-1326-5 - (Nifedipine)

Alphabetical Index


Drug Information of Nifedipine

Product NDC: 54868-1326
Proprietary Name: Nifedipine
Non Proprietary Name: Nifedipine
Active Ingredient(s): 10    mg/1 & nbsp;   Nifedipine
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of Nifedipine

Product NDC: 54868-1326
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072579
Marketing Category: ANDA
Start Marketing Date: 20090129

Package Information of Nifedipine

Package NDC: 54868-1326-5
Package Description: 20 CAPSULE, LIQUID FILLED in 1 BOTTLE (54868-1326-5)

NDC Information of Nifedipine

NDC Code 54868-1326-5
Proprietary Name Nifedipine
Package Description 20 CAPSULE, LIQUID FILLED in 1 BOTTLE (54868-1326-5)
Product NDC 54868-1326
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nifedipine
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20090129
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name NIFEDIPINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient]

Complete Information of Nifedipine


General Information