"72189-105-90" National Drug Code (NDC)

NDC Code	72189-105-90
Package Description	90 TABLET in 1 BOTTLE (72189-105-90)
Product NDC	72189-105
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Pioglitazone
Non-Proprietary Name	Pioglitazone
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20200612
Marketing Category Name	ANDA
Application Number	ANDA200268
Manufacturer	DIRECT RX
Substance Name	PIOGLITAZONE HYDROCHLORIDE
Strength	30
Strength Unit	mg/1
Pharmacy Classes	PPAR alpha [CS], PPAR gamma [CS], Peroxisome Proliferator Receptor alpha Agonist [EPC], Peroxisome Proliferator Receptor gamma Agonist [EPC], Peroxisome Proliferator-activated Receptor Activity [MoA], Thiazolidinedione [EPC], Thiazolidinediones [CS]