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"70518-1757-0" National Drug Code (NDC)

Fluoxetine 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1757-0)
(REMEDYREPACK INC.)

NDC Code70518-1757-0
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1757-0)
Product NDC70518-1757
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFluoxetine
Non-Proprietary NameFluoxetine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190101
Marketing Category NameANDA
Application NumberANDA075755
ManufacturerREMEDYREPACK INC.
Substance NameFLUOXETINE HYDROCHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesSerotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-1757-0





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