Nifedipine - 60429-163-01 - (Nifedipine)

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Drug Information of Nifedipine

Product NDC: 60429-163
Proprietary Name: Nifedipine
Non Proprietary Name: Nifedipine
Active Ingredient(s): 10    mg/1 & nbsp;   Nifedipine
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Nifedipine

Product NDC: 60429-163
Labeler Name: Golden State Medical Supply, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072781
Marketing Category: ANDA
Start Marketing Date: 20090811

Package Information of Nifedipine

Package NDC: 60429-163-01
Package Description: 100 CAPSULE in 1 BOTTLE (60429-163-01)

NDC Information of Nifedipine

NDC Code 60429-163-01
Proprietary Name Nifedipine
Package Description 100 CAPSULE in 1 BOTTLE (60429-163-01)
Product NDC 60429-163
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nifedipine
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20090811
Marketing Category Name ANDA
Labeler Name Golden State Medical Supply, Inc.
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