Strength
75 mg/1
Manufacturer
Alembic Pharmaceuticals Inc.NDC
62332001131
Classification
Generic
Dosage Form
TABLET
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
VENLAFAXINE HYDROCHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA078932On Market Since
10/1/2015
Pharmacological Classes
Norepinephrine Uptake Inhibitors
Serotonin Uptake Inhibitors
Serotonin and Norepinephrine Reuptake Inhibitor
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