"51079-515-20" National Drug Code (NDC)

NDC Code	51079-515-20
Package Description	100 BLISTER PACK in 1 CARTON (51079-515-20) > 1 TABLET in 1 BLISTER PACK (51079-515-01)
Product NDC	51079-515
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Pioglitazone
Non-Proprietary Name	Pioglitazone
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20120906
End Marketing Date	20191031
Marketing Category Name	ANDA
Application Number	ANDA076801
Manufacturer	Mylan Institutional Inc.
Substance Name	PIOGLITAZONE HYDROCHLORIDE
Strength	45
Strength Unit	mg/1
Pharmacy Classes	Peroxisome Proliferator-activated Receptor Activity [MoA],PPAR alpha [CS],PPAR gamma [CS],Thiazolidinedione [EPC],Thiazolidinediones [CS],Peroxisome Proliferator Receptor alpha Agonist [EPC],Peroxisome Proliferator Receptor gamma Agonist [EPC]