Felodipine - 65862-674-90 - (Felodipine)

Alphabetical Index


Drug Information of Felodipine

Product NDC: 65862-674
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: 65862-674
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA203417
Marketing Category: ANDA
Start Marketing Date: 20130117

Package Information of Felodipine

Package NDC: 65862-674-90
Package Description: 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-674-90)

NDC Information of Felodipine

NDC Code 65862-674-90
Proprietary Name Felodipine
Package Description 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-674-90)
Product NDC 65862-674
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Felodipine
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20130117
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
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