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"70518-3820-1" National Drug Code (NDC)

Venlafaxine 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3820-1)
(REMEDYREPACK INC.)

NDC Code70518-3820-1
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3820-1)
Product NDC70518-3820
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVenlafaxine
Non-Proprietary NameVenlafaxine
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20230803
Marketing Category NameANDA
Application NumberANDA214127
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/70518-3820-1





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