FELODIPINE - 64679-414-01 - (FELODIPINE)

Alphabetical Index


Drug Information of FELODIPINE

Product NDC: 64679-414
Proprietary Name: FELODIPINE
Non Proprietary Name: FELODIPINE
Active Ingredient(s): 10    mg/1 & nbsp;   FELODIPINE
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of FELODIPINE

Product NDC: 64679-414
Labeler Name: WOCKHARDT USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091484
Marketing Category: ANDA
Start Marketing Date: 20101205

Package Information of FELODIPINE

Package NDC: 64679-414-01
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64679-414-01)

NDC Information of FELODIPINE

NDC Code 64679-414-01
Proprietary Name FELODIPINE
Package Description 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64679-414-01)
Product NDC 64679-414
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name FELODIPINE
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20101205
Marketing Category Name ANDA
Labeler Name WOCKHARDT USA LLC
Substance Name FELODIPINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient]

Complete Information of FELODIPINE


General Information