"50090-5582-0" National Drug Code (NDC)

NDC Code	50090-5582-0
Package Description	30 TABLET in 1 BOTTLE (50090-5582-0)
Product NDC	50090-5582
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Pioglitazone Hydrochloride
Non-Proprietary Name	Pioglitazone Hydrochloride
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20201028
Marketing Category Name	ANDA
Application Number	ANDA076798
Manufacturer	A-S Medication Solutions
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]