Nifedipine - 0228-2497-10 - (Nifedipine)

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Drug Information of Nifedipine

Product NDC: 0228-2497
Proprietary Name: Nifedipine
Non Proprietary Name: Nifedipine
Active Ingredient(s): 10    mg/1 & nbsp;   Nifedipine
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of Nifedipine

Product NDC: 0228-2497
Labeler Name: Actavis Elizabeth LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072579
Marketing Category: ANDA
Start Marketing Date: 20070102

Package Information of Nifedipine

Package NDC: 0228-2497-10
Package Description: 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (0228-2497-10)

NDC Information of Nifedipine

NDC Code 0228-2497-10
Proprietary Name Nifedipine
Package Description 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (0228-2497-10)
Product NDC 0228-2497
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nifedipine
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20070102
Marketing Category Name ANDA
Labeler Name Actavis Elizabeth LLC
Substance Name NIFEDIPINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient]

Complete Information of Nifedipine


General Information