"66116-504-30" National Drug Code (NDC)

NDC Code	66116-504-30
Package Description	30 TABLET in 1 BOTTLE (66116-504-30)
Product NDC	66116-504
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Pioglitazone
Non-Proprietary Name	Pioglitazone
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20120817
Marketing Category Name	NDA AUTHORIZED GENERIC
Application Number	NDA021073
Manufacturer	MedVantx, Inc.
Substance Name	PIOGLITAZONE HYDROCHLORIDE
Strength	15
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]