"70518-1891-0" National Drug Code (NDC)

Duloxetine 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BLISTER PACK (70518-1891-0)
(REMEDYREPACK INC.)

NDC Code70518-1891-0
Package Description30 CAPSULE, DELAYED RELEASE PELLETS in 1 BLISTER PACK (70518-1891-0)
Product NDC70518-1891
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDuloxetine
Non-Proprietary NameDuloxetine
Dosage FormCAPSULE, DELAYED RELEASE PELLETS
UsageORAL
Start Marketing Date20190221
Marketing Category NameANDA
Application NumberANDA090776
ManufacturerREMEDYREPACK INC.
Substance NameDULOXETINE HYDROCHLORIDE
Strength30
Strength Unitmg/1
Pharmacy ClassesNorepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

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