"68071-2495-1" National Drug Code (NDC)

NDC Code	68071-2495-1
Package Description	120 TABLET in 1 BOTTLE (68071-2495-1)
Product NDC	68071-2495
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	ANDA200044
Manufacturer	NuCare Pharmaceuticals,Inc.
Substance Name	PIOGLITAZONE HYDROCHLORIDE
Strength	30
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]