"70518-2587-0" National Drug Code (NDC)

Venlafaxine Hydrochloride 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2587-0)
(REMEDYREPACK INC.)

NDC Code70518-2587-0
Package Description90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2587-0)
Product NDC70518-2587
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVenlafaxine Hydrochloride
Non-Proprietary NameVenlafaxine Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20200218
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA022104
ManufacturerREMEDYREPACK INC.
Substance NameVENLAFAXINE HYDROCHLORIDE
Strength75
Strength Unitmg/1
Pharmacy ClassesNorepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]

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