"70518-2129-0" National Drug Code (NDC)

NDC Code	70518-2129-0
Package Description	90 TABLET in 1 BOTTLE, PLASTIC (70518-2129-0)
Product NDC	70518-2129
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Pioglitazone
Non-Proprietary Name	Pioglitazone
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20190604
Marketing Category Name	ANDA
Application Number	ANDA200268
Manufacturer	REMEDYREPACK INC.
Substance Name	PIOGLITAZONE HYDROCHLORIDE
Strength	30
Strength Unit	mg/1
Pharmacy Classes	Peroxisome Proliferator Receptor alpha Agonist [EPC], Peroxisome Proliferator Receptor gamma Agonist [EPC], Peroxisome Proliferator-activated Receptor alpha Agonists [MoA], Peroxisome Proliferator-activated Receptor gamma Agonists [MoA], Thiazolidinedione [EPC], Thiazolidinediones [CS]