"16714-645-03" National Drug Code (NDC)

NDC Code	16714-645-03
Package Description	500 TABLET in 1 BOTTLE (16714-645-03)
Product NDC	16714-645
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Pioglitazone
Non-Proprietary Name	Pioglitazone
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20220818
Marketing Category Name	ANDA
Application Number	ANDA202467
Manufacturer	NorthStar RxLLC
Substance Name	PIOGLITAZONE HYDROCHLORIDE
Strength	15
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]