"70518-3083-0" National Drug Code (NDC)

Fluoxetine Hydrochloride 30 TABLET, COATED in 1 BLISTER PACK (70518-3083-0)
(REMEDYREPACK INC.)

NDC Code70518-3083-0
Package Description30 TABLET, COATED in 1 BLISTER PACK (70518-3083-0)
Product NDC70518-3083
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFluoxetine Hydrochloride
Non-Proprietary NameFluoxetine Hydrochloride
Dosage FormTABLET, COATED
UsageORAL
Start Marketing Date20210504
Marketing Category NameANDA
Application NumberANDA203836
ManufacturerREMEDYREPACK INC.
Substance NameFLUOXETINE HYDROCHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesSerotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]

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