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"0904-5379-40" National Drug Code (NDC)

Gemfibrozil 500 TABLET, FILM COATED in 1 BOTTLE (0904-5379-40)
(Major Pharmaceuticals)

NDC Code0904-5379-40
Package Description500 TABLET, FILM COATED in 1 BOTTLE (0904-5379-40)
Product NDC0904-5379
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGemfibrozil
Non-Proprietary NameGemfibrozil
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20040206
Marketing Category NameANDA
Application NumberANDA075034
ManufacturerMajor Pharmaceuticals
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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