"0781-5635-10" National Drug Code (NDC)

NDC Code	0781-5635-10
Package Description	1000 TABLET in 1 BOTTLE (0781-5635-10)
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	GLIMEPIRIDE; PIOGLITAZONE HYDROCHLORIDE
Strength	4; 30
Strength Unit	mg/1; 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], Sulfonylurea Compounds [CS], Sulfonylurea [EPC], Thiazolidinedione [EPC], Thiazolidinediones [CS]