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"70518-2099-0" National Drug Code (NDC)

Cymbalta 30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-2099-0)
(REMEDYREPACK INC.)

NDC Code70518-2099-0
Package Description30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-2099-0)
Product NDC70518-2099
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCymbalta
Non-Proprietary NameDuloxetine Hydrochloride
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20190522
Marketing Category NameNDA
Application NumberNDA021427
ManufacturerREMEDYREPACK INC.
Substance NameDULOXETINE HYDROCHLORIDE
Strength30
Strength Unitmg/1
Pharmacy ClassesNorepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-2099-0





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