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"57664-115-18" National Drug Code (NDC)

Gemfibrozil 1000 TABLET, FILM COATED in 1 BOTTLE (57664-115-18)
(Caraco Pharmaceutical Laboratories, Ltd.)

NDC Code57664-115-18
Package Description1000 TABLET, FILM COATED in 1 BOTTLE (57664-115-18)
Product NDC57664-115
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGemfibrozil
Non-Proprietary NameGemfibrozil
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20090701
Marketing Category NameANDA
Application NumberANDA079239
ManufacturerCaraco Pharmaceutical Laboratories, Ltd.
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/57664-115-18





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