www.ndcvalidator.com
National Drug Code Lookup | NDC Directory | About | Feedback

"0615-8035-39" National Drug Code (NDC)

Duloxetine Hydrochloride 30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (0615-8035-39)
(NCS HealthCare of KY, Inc dba Vangard Labs)

NDC Code0615-8035-39
Package Description30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (0615-8035-39)
Product NDC0615-8035
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
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/0615-8035-39





Copyright © 2007-2024 www.ndcvalidator.com