"0615-8034-39" National Drug Code (NDC)

Duloxetine Hydrochloride 30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (0615-8034-39)
(NCS HealthCare of KY, Inc dba Vangard Labs)

NDC Code0615-8034-39
Package Description30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (0615-8034-39)
Product NDC0615-8034
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDuloxetine Hydrochloride
Non-Proprietary NameDuloxetine Hydrochloride
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20140613
Marketing Category NameANDA
Application NumberANDA202045
ManufacturerNCS HealthCare of KY, Inc dba Vangard Labs
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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