Felodipine - 68462-233-90 - (Felodipine)

Alphabetical Index


Drug Information of Felodipine

Product NDC: 68462-233
Proprietary Name: Felodipine
Non Proprietary Name: Felodipine
Active Ingredient(s): 2.5    mg/1 & nbsp;   Felodipine
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Felodipine

Product NDC: 68462-233
Labeler Name: Glenmark Generics, Inc. USA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090365
Marketing Category: ANDA
Start Marketing Date: 20101220

Package Information of Felodipine

Package NDC: 68462-233-90
Package Description: 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68462-233-90)

NDC Information of Felodipine

NDC Code 68462-233-90
Proprietary Name Felodipine
Package Description 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68462-233-90)
Product NDC 68462-233
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Felodipine
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20101220
Marketing Category Name ANDA
Labeler Name Glenmark Generics, Inc. USA
Substance Name FELODIPINE
Strength Number 2.5
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient]

Complete Information of Felodipine


General Information