"24658-130-18" National Drug Code (NDC)

Gemfibrozil 180 TABLET in 1 BOTTLE (24658-130-18)
(Blu Pharmaceuticals, LLC)

NDC Code24658-130-18
Package Description180 TABLET in 1 BOTTLE (24658-130-18)
Product NDC24658-130
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGemfibrozil
Non-Proprietary NameGemfibrozil
Dosage FormTABLET
UsageORAL
Start Marketing Date20070102
Marketing Category NameANDA
Application NumberANDA077836
ManufacturerBlu Pharmaceuticals, LLC
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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