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"48792-7895-1" National Drug Code (NDC)
Duloxetine 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (48792-7895-1)
(Sunshine Lake Pharma Co., Ltd.)
NDC Code
48792-7895-1
Package Description
60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (48792-7895-1)
Product NDC
48792-7895
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Duloxetine
Non-Proprietary Name
Duloxetine Hydrochloride
Dosage Form
CAPSULE, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
20210211
Marketing Category Name
ANDA
Application Number
ANDA212328
Manufacturer
Sunshine Lake Pharma Co., Ltd.
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/48792-7895-1