"50090-1687-0" National Drug Code (NDC)

NDC Code	50090-1687-0
Package Description	30 TABLET in 1 BOTTLE (50090-1687-0)
Product NDC	50090-1687
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Pioglitazonehydrochloride
Non-Proprietary Name	Pioglitazonehydrochloride
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20130213
Marketing Category Name	ANDA
Application Number	ANDA091298
Manufacturer	A-S Medication Solutions
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 Activity [MoA],PPAR alpha [Chemical/Ingredient],PPAR gamma [Chemical/Ingredient],Thiazolidinedione [EPC],Thiazolidinediones [Chemical/Ingredient]