"71335-0165-1" National Drug Code (NDC)

Duloxetine 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0165-1)
(Bryant Ranch Prepack)

NDC Code71335-0165-1
Package Description30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0165-1)
Product NDC71335-0165
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
Strength20
Strength Unitmg/1
Pharmacy ClassesNorepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]

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