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"52125-818-02" National Drug Code (NDC)
Duloxetine 30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (52125-818-02)
(REMEDYREPACK INC.)
NDC Code
52125-818-02
Package Description
30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (52125-818-02)
Product NDC
52125-818
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Duloxetine
Non-Proprietary Name
Duloxetine
Dosage Form
CAPSULE, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
20140130
Marketing Category Name
ANDA
Application Number
ANDA090745
Manufacturer
REMEDYREPACK INC.
Substance Name
DULOXETINE HYDROCHLORIDE
Strength
20
Strength Unit
mg/1
Pharmacy Classes
Norepinephrine 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/52125-818-02