Felodipine - 13668-132-05 - (Felodipine)

Alphabetical Index


Drug Information of Felodipine

Product NDC: 13668-132
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: 13668-132
Labeler Name: Torrent Pharmaceuticals Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202170
Marketing Category: ANDA
Start Marketing Date: 20111128

Package Information of Felodipine

Package NDC: 13668-132-05
Package Description: 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (13668-132-05)

NDC Information of Felodipine

NDC Code 13668-132-05
Proprietary Name Felodipine
Package Description 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (13668-132-05)
Product NDC 13668-132
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Felodipine
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20111128
Marketing Category Name ANDA
Labeler Name Torrent Pharmaceuticals Limited
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