"60687-905-21" National Drug Code (NDC)

NDC Code	60687-905-21
Package Description	30 BLISTER PACK in 1 CARTON (60687-905-21) / 1 TABLET in 1 BLISTER PACK (60687-905-11)
Product NDC	60687-905
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Pioglitazone
Non-Proprietary Name	Pioglitazone
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20260101
Marketing Category Name	ANDA
Application Number	ANDA077210
Manufacturer	American Health Packaging
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]