Strength
50 mg/1
Manufacturer
Heritage Pharmaceuticals Inc.NDC
23155024809
Classification
Generic
Dosage Form
TABLET
Route
ORAL
Last Updated
5/22/2019
Active Ingredients
VENLAFAXINE HYDROCHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA078554On Market Since
7/19/2021
Pharmacological Classes
Norepinephrine Uptake Inhibitors
Serotonin Uptake Inhibitors
Serotonin and Norepinephrine Reuptake Inhibitor
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