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"71335-0392-1" National Drug Code (NDC)

Duloxetine 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0392-1)
(Bryant Ranch Prepack)

NDC Code71335-0392-1
Package Description30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0392-1)
Product NDC71335-0392
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDuloxetine
Proprietary Name SuffixDelayed-release
Non-Proprietary NameDuloxetine Hydrochloride
Dosage FormCAPSULE, DELAYED RELEASE PELLETS
UsageORAL
Start Marketing Date20140611
Marketing Category NameANDA
Application NumberANDA203088
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/71335-0392-1





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