"71335-1759-2" National Drug Code (NDC)

NDC Code	71335-1759-2
Package Description	90 TABLET in 1 BOTTLE (71335-1759-2)
Product NDC	71335-1759
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Pioglitazone
Non-Proprietary Name	Pioglitazone
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20130213
Marketing Category Name	ANDA
Application Number	ANDA200268
Manufacturer	Bryant Ranch Prepack
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]