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"48792-7896-2" National Drug Code (NDC)

Duloxetine 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (48792-7896-2)
(Sunshine Lake Pharma Co., Ltd.)

NDC Code48792-7896-2
Package Description90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (48792-7896-2)
Product NDC48792-7896
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDuloxetine
Non-Proprietary NameDuloxetine Hydrochloride
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20040824
Marketing Category NameANDA
Application NumberANDA212328
ManufacturerSunshine Lake Pharma Co., Ltd.
Substance NameDULOXETINE HYDROCHLORIDE
Strength30
Strength Unitmg/1
Pharmacy ClassesNorepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

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