"70518-2324-0" National Drug Code (NDC)

NDC Code	70518-2324-0
Package Description	90 TABLET in 1 BOTTLE, PLASTIC (70518-2324-0)
Product NDC	70518-2324
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Pioglitazone
Non-Proprietary Name	Pioglitazone
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20190924
Marketing Category Name	ANDA
Application Number	ANDA078670
Manufacturer	REMEDYREPACK INC.
Substance Name	PIOGLITAZONE HYDROCHLORIDE
Strength	30
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]