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"71335-2017-8" National Drug Code (NDC)

Duloxetine 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-8)
(Bryant Ranch Prepack)

NDC Code71335-2017-8
Package Description120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-8)
Product NDC71335-2017
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDuloxetine
Non-Proprietary NameDuloxetine
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20170316
Marketing Category NameANDA
Application NumberANDA208706
ManufacturerBryant Ranch Prepack
Substance NameDULOXETINE HYDROCHLORIDE
Strength30
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/71335-2017-8





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