"24658-260-90" National Drug Code (NDC)

Gemfibrozil 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (24658-260-90)
(PuraCap Laboratories LLC dba Blu Pharmaceuticals)

NDC Code24658-260-90
Package Description90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (24658-260-90)
Product NDC24658-260
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGemfibrozil
Non-Proprietary NameGemfibrozil
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20110401
Marketing Category NameANDA
Application NumberANDA078012
ManufacturerPuraCap Laboratories LLC dba Blu Pharmaceuticals
Substance NameGEMFIBROZIL
Strength600
Strength Unitmg/1
Pharmacy ClassesPPAR alpha [CS], Peroxisome Proliferator Receptor alpha Agonist [EPC], Peroxisome Proliferator-activated Receptor alpha Agonists [MoA]

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