"57237-220-05" National Drug Code (NDC)

NDC Code	57237-220-05
Package Description	500 TABLET in 1 BOTTLE (57237-220-05)
Product NDC	57237-220
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	Rising Pharma Holdings, Inc.
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]