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"0615-8204-39" National Drug Code (NDC)
Duloxetine Hydrochloride 30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (0615-8204-39)
(NCS HealthCare of KY, LLC dba Vangard Labs)
NDC Code
0615-8204-39
Package Description
30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (0615-8204-39)
Product NDC
0615-8204
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Duloxetine Hydrochloride
Non-Proprietary Name
Duloxetin Hydrochloride
Dosage Form
CAPSULE, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
20131211
End Marketing Date
20240930
Marketing Category Name
ANDA
Application Number
ANDA090774
Manufacturer
NCS HealthCare of KY, LLC dba Vangard Labs
Substance Name
DULOXETINE HYDROCHLORIDE
Strength
60
Strength Unit
mg/1
Pharmacy Classes
Norepinephrine 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/0615-8204-39