Actos - 49999-449-30 - (pioglitazone hydrochloride)

Alphabetical Index


Drug Information of Actos

Product NDC: 49999-449
Proprietary Name: Actos
Non Proprietary Name: pioglitazone hydrochloride
Active Ingredient(s): 15    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: 49999-449
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021073
Marketing Category: NDA
Start Marketing Date: 20120217

Package Information of Actos

Package NDC: 49999-449-30
Package Description: 30 TABLET in 1 BOTTLE (49999-449-30)

NDC Information of Actos

NDC Code 49999-449-30
Proprietary Name Actos
Package Description 30 TABLET in 1 BOTTLE (49999-449-30)
Product NDC 49999-449
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name pioglitazone hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120217
Marketing Category Name NDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name PIOGLITAZONE HYDROCHLORIDE
Strength Number 15
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