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Nifediac CC - 0093-1023-01 - (Nifedipine)

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Drug Information of Nifediac CC

Product NDC: 0093-1023
Proprietary Name: Nifediac CC
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 Nifediac CC

Product NDC: 0093-1023
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076070
Marketing Category: ANDA
Start Marketing Date: 20020916

Package Information of Nifediac CC

Package NDC: 0093-1023-01
Package Description: 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-1023-01)

NDC Information of Nifediac CC

NDC Code 0093-1023-01
Proprietary Name Nifediac CC
Package Description 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-1023-01)
Product NDC 0093-1023
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nifedipine
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20020916
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA 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 Nifediac CC


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