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"0615-7895-39" National Drug Code (NDC)

Duloxetine Hydrochloride 30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (0615-7895-39)
(NCS HealthCare of KY, Inc dba Vangard Labs)

NDC Code0615-7895-39
Package Description30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (0615-7895-39)
Product NDC0615-7895
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDuloxetine Hydrochloride
Non-Proprietary NameDuloxetin Hydrochloride
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20131211
Marketing Category NameANDA
Application NumberANDA090774
ManufacturerNCS HealthCare of KY, Inc dba Vangard Labs
Substance NameDULOXETINE HYDROCHLORIDE
Strength60
Strength Unitmg/1
Pharmacy ClassesNorepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0615-7895-39





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