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Nifediac CC - 0093-5272-55 - (Nifedipine)

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Drug Information of Nifediac CC

Product NDC: 0093-5272
Proprietary Name: Nifediac CC
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 Nifediac CC

Product NDC: 0093-5272
Labeler Name: TEVA PHARMACEUTICALS USA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075269
Marketing Category: ANDA
Start Marketing Date: 20040109

Package Information of Nifediac CC

Package NDC: 0093-5272-55
Package Description: 300 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-5272-55)

NDC Information of Nifediac CC

NDC Code 0093-5272-55
Proprietary Name Nifediac CC
Package Description 300 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-5272-55)
Product NDC 0093-5272
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nifedipine
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20040109
Marketing Category Name ANDA
Labeler Name TEVA PHARMACEUTICALS USA
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 Nifediac CC


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