"70518-2059-0" National Drug Code (NDC)

NDC Code	70518-2059-0
Package Description	30 POUCH in 1 BOX (70518-2059-0) > 1 TABLET in 1 POUCH (70518-2059-1)
Product NDC	70518-2059
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Pioglitazonehydrochloride
Non-Proprietary Name	Pioglitazonehydrochloride
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20190502
Marketing Category Name	ANDA
Application Number	ANDA091298
Manufacturer	REMEDYREPACK 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]