"58118-5420-1" National Drug Code (NDC)

NDC Code	58118-5420-1
Package Description	180 TABLET in 1 BOTTLE (58118-5420-1)
Product NDC	58118-5420
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Pioglitazone
Non-Proprietary Name	Pioglitazone
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20130301
Marketing Category Name	ANDA
Application Number	ANDA078670
Manufacturer	Clinical Solutions Wholesale
Substance Name	PIOGLITAZONE HYDROCHLORIDE
Strength	15
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]