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"70518-3219-0" National Drug Code (NDC)

Venlafaxine Hydrochloride 30 TABLET in 1 BLISTER PACK (70518-3219-0)
(REMEDYREPACK INC.)

NDC Code70518-3219-0
Package Description30 TABLET in 1 BLISTER PACK (70518-3219-0)
Product NDC70518-3219
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVenlafaxine Hydrochloride
Non-Proprietary NameVenlafaxine Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20210913
Marketing Category NameANDA
Application NumberANDA076690
ManufacturerREMEDYREPACK INC.
Substance NameVENLAFAXINE HYDROCHLORIDE
Strength75
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/70518-3219-0





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