ANTARA - 27437-109-06 - (FENOFIBRATE)

Alphabetical Index


Drug Information of ANTARA

Product NDC: 27437-109
Proprietary Name: ANTARA
Non Proprietary Name: FENOFIBRATE
Active Ingredient(s): 43    mg/1 & nbsp;   FENOFIBRATE
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of ANTARA

Product NDC: 27437-109
Labeler Name: LUPIN PHARMA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021695
Marketing Category: NDA
Start Marketing Date: 20090925

Package Information of ANTARA

Package NDC: 27437-109-06
Package Description: 30 CAPSULE in 1 BOTTLE (27437-109-06)

NDC Information of ANTARA

NDC Code 27437-109-06
Proprietary Name ANTARA
Package Description 30 CAPSULE in 1 BOTTLE (27437-109-06)
Product NDC 27437-109
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name FENOFIBRATE
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20090925
Marketing Category Name NDA
Labeler Name LUPIN PHARMA
Substance Name FENOFIBRATE
Strength Number 43
Strength Unit mg/1
Pharmaceutical Classes Peroxisome Proliferator Receptor alpha Agonist [EPC],Peroxisome Proliferator-activated Receptor alpha Agonists [MoA],PPAR alpha [Chemical/Ingredient]

Complete Information of ANTARA


General Information