"60505-2996-8" National Drug Code (NDC)

Duloxetine Hydrochloride 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (60505-2996-8)
(Apotex Corp.)

NDC Code60505-2996-8
Package Description1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (60505-2996-8)
Product NDC60505-2996
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDuloxetine Hydrochloride
Non-Proprietary NameDuloxetine Hydrochloride
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20140613
Marketing Category NameANDA
Application NumberANDA202045
ManufacturerApotex Corp.
Substance NameDULOXETINE HYDROCHLORIDE
Strength30
Strength Unitmg/1
Pharmacy ClassesNorepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

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