"51079-787-19" National Drug Code (NDC)

NDC Code	51079-787-19
Package Description	25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-787-19) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-787-17)
Product NDC	51079-787
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Gemfibrozil
Non-Proprietary Name	Gemfibrozil
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	19960201
Marketing Category Name	ANDA
Application Number	ANDA074256
Manufacturer	Mylan Institutional 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]