"0781-5635-06" National Drug Code (NDC)

NDC Code	0781-5635-06
Package Description	7 CARTON in 1 BLISTER PACK (0781-5635-06) > 28 TABLET in 1 CARTON (0781-5635-08)
Product NDC	0781-5635
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Pioglitazone Hydrochloride And Glimepiride
Non-Proprietary Name	Pioglitazone Hydrochloride And Glimepiride
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20130108
Marketing Category Name	ANDA
Application Number	ANDA201049
Manufacturer	Sandoz Inc
Substance Name	PIOGLITAZONE HYDROCHLORIDE; GLIMEPIRIDE
Strength	30; 4
Strength Unit	mg/1; 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],Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]