"0591-3207-19" National Drug Code (NDC)

NDC Code	0591-3207-19
Package Description	90 TABLET in 1 BOTTLE, PLASTIC (0591-3207-19)
Product NDC	0591-3207
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Pioglitazone Hydrochloride
Non-Proprietary Name	Pioglitazone Hydrochloride
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20121026
Marketing Category Name	ANDA
Application Number	ANDA076798
Manufacturer	Actavis Pharma, 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]