"71335-1137-3" National Drug Code (NDC)

NDC Code	71335-1137-3
Package Description	60 TABLET in 1 BOTTLE (71335-1137-3)
Product NDC	71335-1137
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Pioglitazone
Non-Proprietary Name	Pioglitazone
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20150204
Marketing Category Name	ANDA
Application Number	ANDA077210
Manufacturer	Bryant Ranch Prepack
Substance Name	PIOGLITAZONE HYDROCHLORIDE
Strength	15
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]