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"70518-0937-7" National Drug Code (NDC)

Duloxetine 180 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-0937-7)
(REMEDYREPACK INC.)

NDC Code70518-0937-7
Package Description180 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-0937-7)
Product NDC70518-0937
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDuloxetine
Non-Proprietary NameDuloxetine Hydrochloride
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20190425
Marketing Category NameANDA
Application NumberANDA090778
ManufacturerREMEDYREPACK INC.
Substance NameDULOXETINE HYDROCHLORIDE
Strength60
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/70518-0937-7





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