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"24658-130-05" National Drug Code (NDC)

Gemfibrozil 500 TABLET in 1 BOTTLE (24658-130-05)
(Blu Pharmaceuticals, LLC)

NDC Code24658-130-05
Package Description500 TABLET in 1 BOTTLE (24658-130-05)
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/24658-130-05





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