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"70518-1385-0" National Drug Code (NDC)

Venlafaxine 30 TABLET in 1 BLISTER PACK (70518-1385-0)
(REMEDYREPACK INC.)

NDC Code70518-1385-0
Package Description30 TABLET in 1 BLISTER PACK (70518-1385-0)
Product NDC70518-1385
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVenlafaxine
Non-Proprietary NameVenlafaxine Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20180824
Marketing Category NameANDA
Application NumberANDA090555
ManufacturerREMEDYREPACK INC.
Substance NameVENLAFAXINE HYDROCHLORIDE
Strength37.5
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/70518-1385-0





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