Strength
37.5 mg/1
Manufacturer
Sun Pharmaceutical Industries Inc.NDC
47335076081
Classification
Generic
Dosage Form
TABLET, EXTENDED RELEASE
Route
ORAL
Last Updated
2/18/2026
Active Ingredients
VENLAFAXINE HYDROCHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA091272On Market Since
12/15/2014
Pharmacological Classes
Norepinephrine Uptake Inhibitors
Serotonin Uptake Inhibitors
Serotonin and Norepinephrine Reuptake Inhibitor
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