Actos - 54868-4354-1 - (pioglitazone hydrochloride)

Alphabetical Index


Drug Information of Actos

Product NDC: 54868-4354
Proprietary Name: Actos
Non Proprietary Name: pioglitazone hydrochloride
Active Ingredient(s): 30    mg/1 & nbsp;   pioglitazone hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Actos

Product NDC: 54868-4354
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021073
Marketing Category: NDA
Start Marketing Date: 20050304

Package Information of Actos

Package NDC: 54868-4354-1
Package Description: 90 TABLET in 1 BOTTLE (54868-4354-1)

NDC Information of Actos

NDC Code 54868-4354-1
Proprietary Name Actos
Package Description 90 TABLET in 1 BOTTLE (54868-4354-1)
Product NDC 54868-4354
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name pioglitazone hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20050304
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name PIOGLITAZONE HYDROCHLORIDE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes Peroxisome Proliferator Receptor alpha Agonist [EPC],Peroxisome Proliferator Receptor gamma Agonist [EPC],Peroxisome Proliferator-activated Receptor Activity [MoA],PPAR alpha [Chemical/Ingredient],PPAR gamma [Chemical/Ingredient],Thiazolidinedione [EPC],Thiazolidinediones [Chemical/Ingredient]

Complete Information of Actos


General Information