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"80175-0582-3" National Drug Code (NDC)

Duloxetine 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80175-0582-3)
(Central Packaging)

NDC Code80175-0582-3
Package Description30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80175-0582-3)
Product NDC80175-0582
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDuloxetine
Non-Proprietary NameDuloxetine
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20160811
Marketing Category NameANDA
Application NumberANDA204343
ManufacturerCentral Packaging
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/80175-0582-3





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