"50090-3317-0" National Drug Code (NDC)

Duloxetine Hydrochloride 33 BLISTER PACK in 1 BOX, UNIT-DOSE (50090-3317-0) > 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
(A-S Medication Solutions)

NDC Code50090-3317-0
Package Description33 BLISTER PACK in 1 BOX, UNIT-DOSE (50090-3317-0) > 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
Product NDC50090-3317
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
ManufacturerA-S Medication Solutions
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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