"60505-2997-3" National Drug Code (NDC)

Duloxetine Hydrochloride 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (60505-2997-3)
(Apotex Corp.)

NDC Code60505-2997-3
Package Description30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (60505-2997-3)
Product NDC60505-2997
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDuloxetine Hydrochloride
Non-Proprietary NameDuloxetine Hydrochloride
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20140613
End Marketing Date20230630
Marketing Category NameANDA
Application NumberANDA202045
ManufacturerApotex Corp.
Substance NameDULOXETINE HYDROCHLORIDE
Strength60
Strength Unitmg/1
Pharmacy ClassesNorepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]

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