"0378-0318-05" National Drug Code (NDC)

NDC Code	0378-0318-05
Package Description	500 TABLET in 1 BOTTLE, PLASTIC (0378-0318-05)
Product NDC	0378-0318
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Pioglitazone
Non-Proprietary Name	Pioglitazone
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20120817
End Marketing Date	20200131
Marketing Category Name	ANDA
Application Number	ANDA076801
Manufacturer	Mylan Pharmaceuticals 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]