"65580-301-03" National Drug Code (NDC)

Venlafaxine Hydrochloride 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65580-301-03)
(Upstate Pharma, LLC)

NDC Code65580-301-03
Package Description30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65580-301-03)
Product NDC65580-301
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVenlafaxine Hydrochloride
Non-Proprietary NameVenlafaxine Hydrochloride
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20080930
End Marketing Date20171231
Marketing Category NameNDA
Application NumberNDA022104
ManufacturerUpstate Pharma, LLC
Substance NameVENLAFAXINE HYDROCHLORIDE
Strength37.5
Strength Unitmg/1
Pharmacy ClassesNorepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

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