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"0615-8203-39" National Drug Code (NDC)

Duloxetine Hydrochloride 30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (0615-8203-39)
(NCS HealthCare of KY, LLC dba Vangard Labs)

NDC Code0615-8203-39
Package Description30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (0615-8203-39)
Product NDC0615-8203
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDuloxetine Hydrochloride
Non-Proprietary NameDuloxetin Hydrochloride
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20131211
End Marketing Date20240930
Marketing Category NameANDA
Application NumberANDA090774
ManufacturerNCS HealthCare of KY, LLC dba Vangard Labs
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/0615-8203-39





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