"0093-2048-05" National Drug Code (NDC)

NDC Code	0093-2048-05
Package Description	500 TABLET in 1 BOTTLE (0093-2048-05)
Product NDC	0093-2048
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Pioglitazone
Non-Proprietary Name	Pioglitazone
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20120817
Marketing Category Name	NDA AUTHORIZED GENERIC
Application Number	NDA021073
Manufacturer	Teva Pharmaceuticals USA Inc
Substance Name	PIOGLITAZONE HYDROCHLORIDE
Strength	15
Strength Unit	mg/1
Pharmacy Classes	Peroxisome Proliferator-activated Receptor Activity [MoA],PPAR alpha [CS],PPAR gamma [CS],Thiazolidinedione [EPC],Thiazolidinediones [CS],Peroxisome Proliferator Receptor alpha Agonist [EPC],Peroxisome Proliferator Receptor gamma Agonist [EPC]