"67253-741-50" National Drug Code (NDC)

NDC Code	67253-741-50
Package Description	500 TABLET, FILM COATED in 1 BOTTLE (67253-741-50)
Product NDC	67253-741
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Gemfibrozil
Non-Proprietary Name	Gemfibrozil
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	19930927
End Marketing Date	20180331
Marketing Category Name	ANDA
Application Number	ANDA074270
Manufacturer	DAVA Pharmaceuticals, Inc.
Substance Name	GEMFIBROZIL
Strength	600
Strength Unit	mg/1
Pharmacy Classes	Peroxisome Proliferator Receptor alpha Agonist [EPC],Peroxisome Proliferator-activated Receptor alpha Agonists [MoA],PPAR alpha [Chemical/Ingredient]