Discontinued
Strength
37.5 mg/1
Manufacturer
Vertical Pharmaceuticals, LLCNDC
68025007930
Classification
Generic
Dosage Form
TABLET, EXTENDED RELEASE
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
VENLAFAXINE HYDROCHLORIDEApproval Type
Authorized Generic (NDA)
FDA Application
NDA022104On Market Since
4/29/2010
Pharmacological Classes
Norepinephrine Uptake Inhibitors
Serotonin Uptake Inhibitors
Serotonin and Norepinephrine Reuptake Inhibitor
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