nifedipine - 54868-4875-2 - (nifedipine)

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Drug Information of nifedipine

Product NDC: 54868-4875
Proprietary Name: nifedipine
Non Proprietary Name: nifedipine
Active Ingredient(s): 90    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: 54868-4875
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019684
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20030811

Package Information of nifedipine

Package NDC: 54868-4875-2
Package Description: 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (54868-4875-2)

NDC Information of nifedipine

NDC Code 54868-4875-2
Proprietary Name nifedipine
Package Description 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (54868-4875-2)
Product NDC 54868-4875
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name nifedipine
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20030811
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Physicians Total Care, Inc.
Substance Name NIFEDIPINE
Strength Number 90
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient]

Complete Information of nifedipine


General Information