"59115-094-55" National Drug Code (NDC)

Gemfibrozil 500 TABLET, FILM COATED in 1 BOTTLE (59115-094-55)
(Hikma Pharmaceutical)

NDC Code59115-094-55
Package Description500 TABLET, FILM COATED in 1 BOTTLE (59115-094-55)
Product NDC59115-094
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGemfibrozil
Non-Proprietary NameGemfibrozil
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20100816
Marketing Category NameANDA
Application NumberANDA078599
ManufacturerHikma Pharmaceutical
Substance NameGEMFIBROZIL
Strength600
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator-activated Receptor alpha Agonists [MoA],PPAR alpha [CS],Peroxisome Proliferator Receptor alpha Agonist [EPC]

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