nifedipine - 55154-5979-4 - (nifedipine)

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Drug Information of nifedipine

Product NDC: 55154-5979
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: 55154-5979
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072579
Marketing Category: ANDA
Start Marketing Date: 19910108

Package Information of nifedipine

Package NDC: 55154-5979-4
Package Description: 100 POUCH in 1 CARTON (55154-5979-4) > 1 CAPSULE, LIQUID FILLED in 1 POUCH (55154-5979-6)

NDC Information of nifedipine

NDC Code 55154-5979-4
Proprietary Name nifedipine
Package Description 100 POUCH in 1 CARTON (55154-5979-4) > 1 CAPSULE, LIQUID FILLED in 1 POUCH (55154-5979-6)
Product NDC 55154-5979
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name nifedipine
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 19910108
Marketing Category Name ANDA
Labeler Name Cardinal Health
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


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