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"70518-1139-0" National Drug Code (NDC)

Duloxetine 30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-1139-0)
(REMEDYREPACK INC.)

NDC Code70518-1139-0
Package Description30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-1139-0)
Product NDC70518-1139
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDuloxetine
Non-Proprietary NameDuloxetine
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20180425
Marketing Category NameANDA
Application NumberANDA208706
ManufacturerREMEDYREPACK INC.
Substance NameDULOXETINE HYDROCHLORIDE
Strength20
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/70518-1139-0





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