"0781-5422-10" National Drug Code (NDC)

NDC Code	0781-5422-10
Package Description	1000 TABLET in 1 BOTTLE (0781-5422-10)
Product NDC	0781-5422
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Pioglitazone
Non-Proprietary Name	Pioglitazone
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20130301
Marketing Category Name	ANDA
Application Number	ANDA078670
Manufacturer	Sandoz Inc
Substance Name	PIOGLITAZONE HYDROCHLORIDE
Strength	45
Strength Unit	mg/1
Pharmacy Classes	PPAR alpha [CS], PPAR gamma [CS], Peroxisome Proliferator Receptor alpha Agonist [EPC], Peroxisome Proliferator Receptor gamma Agonist [EPC], Peroxisome Proliferator-activated Receptor Activity [MoA], Thiazolidinedione [EPC], Thiazolidinediones [CS]