Actos - 64764-301-15 - (pioglitazone)

Alphabetical Index


Drug Information of Actos

Product NDC: 64764-301
Proprietary Name: Actos
Non Proprietary Name: pioglitazone
Active Ingredient(s): 30    mg/1 & nbsp;   pioglitazone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Actos

Product NDC: 64764-301
Labeler Name: Takeda Pharmaceuticals America, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021073
Marketing Category: NDA
Start Marketing Date: 19990715

Package Information of Actos

Package NDC: 64764-301-15
Package Description: 90 TABLET in 1 BOTTLE (64764-301-15)

NDC Information of Actos

NDC Code 64764-301-15
Proprietary Name Actos
Package Description 90 TABLET in 1 BOTTLE (64764-301-15)
Product NDC 64764-301
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name pioglitazone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19990715
Marketing Category Name NDA
Labeler Name Takeda Pharmaceuticals America, 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