Nifedical - 0093-5173-55 - (nifedipine)

Alphabetical Index


Drug Information of Nifedical

Product NDC: 0093-5173
Proprietary Name: Nifedical
Non Proprietary Name: nifedipine
Active Ingredient(s): 60    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 Nifedical

Product NDC: 0093-5173
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075289
Marketing Category: ANDA
Start Marketing Date: 20001211

Package Information of Nifedical

Package NDC: 0093-5173-55
Package Description: 300 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-5173-55)

NDC Information of Nifedical

NDC Code 0093-5173-55
Proprietary Name Nifedical
Package Description 300 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-5173-55)
Product NDC 0093-5173
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name nifedipine
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20001211
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name NIFEDIPINE
Strength Number 60
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient]

Complete Information of Nifedical


General Information