Nifedipine - 0615-5541-39 - (nifedipine)

Alphabetical Index


Drug Information of Nifedipine

Product NDC: 0615-5541
Proprietary Name: Nifedipine
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 Nifedipine

Product NDC: 0615-5541
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090649
Marketing Category: ANDA
Start Marketing Date: 20100630

Package Information of Nifedipine

Package NDC: 0615-5541-39
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0615-5541-39)

NDC Information of Nifedipine

NDC Code 0615-5541-39
Proprietary Name Nifedipine
Package Description 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0615-5541-39)
Product NDC 0615-5541
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name nifedipine
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20100630
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
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 Nifedipine


General Information