"70934-761-90" National Drug Code (NDC)

Venlafaxine 90 TABLET in 1 BOTTLE, PLASTIC (70934-761-90)
(Denton Pharma, Inc. DBA Northwind Pharmaceuticals)

NDC Code70934-761-90
Package Description90 TABLET in 1 BOTTLE, PLASTIC (70934-761-90)
Product NDC70934-761
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVenlafaxine
Non-Proprietary NameVenlafaxine
Dosage FormTABLET
UsageORAL
Start Marketing Date20200529
End Marketing Date20240831
Marketing Category NameANDA
Application NumberANDA078932
ManufacturerDenton Pharma, Inc. DBA Northwind Pharmaceuticals
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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