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"23155-655-10" National Drug Code (NDC)

Duloxetine 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (23155-655-10)
(Heritage Pharmaceuticals Inc.)

NDC Code23155-655-10
Package Description1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (23155-655-10)
Product NDC23155-655
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDuloxetine
Non-Proprietary NameDuloxetine
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20180622
Marketing Category NameANDA
Application NumberANDA202336
ManufacturerHeritage Pharmaceuticals Inc.
Substance NameDULOXETINE HYDROCHLORIDE
Strength30
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/23155-655-10





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