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"82009-173-90" National Drug Code (NDC)

Duloxetine 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (82009-173-90)
(Quallent Pharmaceuticals Health LLC)

NDC Code82009-173-90
Package Description1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (82009-173-90)
Product NDC82009-173
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDuloxetine
Non-Proprietary NameDuloxetine
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20250701
Marketing Category NameANDA
Application NumberANDA208706
ManufacturerQuallent Pharmaceuticals Health LLC
Substance NameDULOXETINE HYDROCHLORIDE
Strength60
Strength Unitmg/1
Pharmacy ClassesNorepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/82009-173-90





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