nifedipine - 63629-4089-1 - (nifedipine)

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Drug Information of nifedipine

Product NDC: 63629-4089
Proprietary Name: nifedipine
Non Proprietary Name: nifedipine
Active Ingredient(s): 30    mg/1 & nbsp;   nifedipine
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of nifedipine

Product NDC: 63629-4089
Labeler Name: bryant ranch prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075128
Marketing Category: ANDA
Start Marketing Date: 20091005

Package Information of nifedipine

Package NDC: 63629-4089-1
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-4089-1)

NDC Information of nifedipine

NDC Code 63629-4089-1
Proprietary Name nifedipine
Package Description 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-4089-1)
Product NDC 63629-4089
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name nifedipine
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20091005
Marketing Category Name ANDA
Labeler Name bryant ranch prepack
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


General Information