"50090-6874-0" National Drug Code (NDC)

NDC Code	50090-6874-0
Package Description	90 TABLET in 1 BOTTLE (50090-6874-0)
Product NDC	50090-6874
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	A-S Medication Solutions
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]