Felodipine - 53489-369-01 - (Felodipine)

Alphabetical Index


Drug Information of Felodipine

Product NDC: 53489-369
Proprietary Name: Felodipine
Non Proprietary Name: Felodipine
Active Ingredient(s): 5    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: 53489-369
Labeler Name: Mutual Pharmaceutical Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075896
Marketing Category: ANDA
Start Marketing Date: 20041102

Package Information of Felodipine

Package NDC: 53489-369-01
Package Description: 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (53489-369-01)

NDC Information of Felodipine

NDC Code 53489-369-01
Proprietary Name Felodipine
Package Description 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (53489-369-01)
Product NDC 53489-369
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Felodipine
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20041102
Marketing Category Name ANDA
Labeler Name Mutual Pharmaceutical Company, Inc.
Substance Name FELODIPINE
Strength Number 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