"63629-3299-3" National Drug Code (NDC)

NDC Code	63629-3299-3
Package Description	90 TABLET in 1 BOTTLE (63629-3299-3)
Product NDC	63629-3299
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Pioglitazone Hydrochloride
Non-Proprietary Name	Pioglitazone Hydrochloride
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20130213
End Marketing Date	20250731
Marketing Category Name	ANDA
Application Number	ANDA200044
Manufacturer	Bryant Ranch Prepack
Substance Name	PIOGLITAZONE HYDROCHLORIDE
Strength	30
Strength Unit	mg/1
Pharmacy Classes	Peroxisome Proliferator Receptor alpha Agonist [EPC], Peroxisome Proliferator Receptor gamma Agonist [EPC], Peroxisome Proliferator-activated Receptor alpha Agonists [MoA], Peroxisome Proliferator-activated Receptor gamma Agonists [MoA], Thiazolidinedione [EPC], Thiazolidinediones [CS]