Procardia - 55154-2706-0 - (nifedipine)

Alphabetical Index


Drug Information of Procardia

Product NDC: 55154-2706
Proprietary Name: Procardia
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 Procardia

Product NDC: 55154-2706
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019684
Marketing Category: NDA
Start Marketing Date: 19890906

Package Information of Procardia

Package NDC: 55154-2706-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-2706-0) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of Procardia

NDC Code 55154-2706-0
Proprietary Name Procardia
Package Description 10 BLISTER PACK in 1 BAG (55154-2706-0) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 55154-2706
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name nifedipine
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19890906
Marketing Category Name NDA
Labeler Name Cardinal Health
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 Procardia


General Information