"70518-1818-0" National Drug Code (NDC)

NDC Code	70518-1818-0
Package Description	30 TABLET in 1 BLISTER PACK (70518-1818-0)
Product NDC	70518-1818
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Pioglitazone Hydrochloride
Non-Proprietary Name	Pioglitazone Hydrochloride
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20190124
Marketing Category Name	ANDA
Application Number	ANDA200044
Manufacturer	REMEDYREPACK 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]