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"70518-1802-3" National Drug Code (NDC)

Duloxetine 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (70518-1802-3)
(REMEDYREPACK INC.)

NDC Code70518-1802-3
Package Description90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (70518-1802-3)
Product NDC70518-1802
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDuloxetine
Proprietary Name SuffixDelayed-release
Non-Proprietary NameDuloxetine Hydrochloride
Dosage FormCAPSULE, DELAYED RELEASE PELLETS
UsageORAL
Start Marketing Date20190117
Marketing Category NameANDA
Application NumberANDA203088
ManufacturerREMEDYREPACK INC.
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/70518-1802-3





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