Nifedipine - 21695-909-30 - (Nifedipine)

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Drug Information of Nifedipine

Product NDC: 21695-909
Proprietary Name: Nifedipine
Non Proprietary Name: Nifedipine
Active Ingredient(s): 60    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: 21695-909
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077899
Marketing Category: ANDA
Start Marketing Date: 20061213

Package Information of Nifedipine

Package NDC: 21695-909-30
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (21695-909-30)

NDC Information of Nifedipine

NDC Code 21695-909-30
Proprietary Name Nifedipine
Package Description 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (21695-909-30)
Product NDC 21695-909
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nifedipine
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20061213
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
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