"16729-022-16" National Drug Code (NDC)

NDC Code	16729-022-16
Package Description	500 TABLET in 1 BOTTLE (16729-022-16)
Product NDC	16729-022
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Pioglitazone
Non-Proprietary Name	Pioglitazone
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20130213
End Marketing Date	20250930
Marketing Category Name	ANDA
Application Number	ANDA200044
Manufacturer	Accord Healthcare, Inc.
Substance Name	PIOGLITAZONE HYDROCHLORIDE
Strength	45
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]