Triglide - 59630-485-30 - (fenofibrate)

Alphabetical Index


Drug Information of Triglide

Product NDC: 59630-485
Proprietary Name: Triglide
Non Proprietary Name: fenofibrate
Active Ingredient(s): 160    mg/1 & nbsp;   fenofibrate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Triglide

Product NDC: 59630-485
Labeler Name: Shionogi Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021350
Marketing Category: NDA
Start Marketing Date: 20050507

Package Information of Triglide

Package NDC: 59630-485-30
Package Description: 1 BOTTLE in 1 CARTON (59630-485-30) > 30 TABLET in 1 BOTTLE

NDC Information of Triglide

NDC Code 59630-485-30
Proprietary Name Triglide
Package Description 1 BOTTLE in 1 CARTON (59630-485-30) > 30 TABLET in 1 BOTTLE
Product NDC 59630-485
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fenofibrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20050507
Marketing Category Name NDA
Labeler Name Shionogi Inc.
Substance Name FENOFIBRATE
Strength Number 160
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 Triglide


General Information