"53002-2757-3" National Drug Code (NDC)

NDC Code	53002-2757-3
Package Description	30 TABLET in 1 BOTTLE (53002-2757-3)
Product NDC	53002-2757
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Pioglitazone
Non-Proprietary Name	Pioglitazone
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20150522
Marketing Category Name	ANDA
Application Number	ANDA077210
Manufacturer	RPK Pharmaceuticals, Inc.
Substance Name	PIOGLITAZONE HYDROCHLORIDE
Strength	45
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]