"61786-565-19" National Drug Code (NDC)

NDC Code	61786-565-19
Package Description	90 TABLET in 1 BOTTLE (61786-565-19)
Product NDC	61786-565
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Pioglitazone Hydrochloride
Non-Proprietary Name	Pioglitazone Hydrochloride
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20160125
Marketing Category Name	ANDA
Application Number	ANDA200044
Manufacturer	REMEDYREPACK INC.
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 Activity [MoA],PPAR alpha [Chemical/Ingredient],PPAR gamma [Chemical/Ingredient],Thiazolidinedione [EPC],Thiazolidinediones [Chemical/Ingredient]