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"24658-260-18" National Drug Code (NDC)

Gemfibrozil 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (24658-260-18)
(PuraCap Laboratories LLC dba Blu Pharmaceuticals)

NDC Code24658-260-18
Package Description180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (24658-260-18)
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/24658-260-18





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