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"16714-422-05" National Drug Code (NDC)

Duloxetine Hydrochloride 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (16714-422-05)
(NorthStar RxLLC)

NDC Code16714-422-05
Package Description1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (16714-422-05)
Product NDC16714-422
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDuloxetine Hydrochloride
Proprietary Name Suffix20 Mg
Non-Proprietary NameDuloxetine
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20140609
Marketing Category NameANDA
Application NumberANDA202949
ManufacturerNorthStar RxLLC
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/16714-422-05





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