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"48792-7897-2" National Drug Code (NDC)

Duloxetine 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (48792-7897-2)
(Sunshine Lake Pharma Co., Ltd.)

NDC Code48792-7897-2
Package Description90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (48792-7897-2)
Product NDC48792-7897
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDuloxetine
Non-Proprietary NameDuloxetine Hydrochloride
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20100115
Marketing Category NameANDA
Application NumberANDA212328
ManufacturerSunshine Lake Pharma Co., Ltd.
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/48792-7897-2





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