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"67253-741-06" National Drug Code (NDC)

Gemfibrozil 60 TABLET, FILM COATED in 1 BOTTLE (67253-741-06)
(DAVA Pharmaceuticals, Inc.)

NDC Code67253-741-06
Package Description60 TABLET, FILM COATED in 1 BOTTLE (67253-741-06)
Product NDC67253-741
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGemfibrozil
Non-Proprietary NameGemfibrozil
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date19930927
End Marketing Date20180331
Marketing Category NameANDA
Application NumberANDA074270
ManufacturerDAVA Pharmaceuticals, Inc.
Substance NameGEMFIBROZIL
Strength600
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC],Peroxisome Proliferator-activated Receptor alpha Agonists [MoA],PPAR alpha [Chemical/Ingredient]

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