Strength
37.5 mg/1
Manufacturer
Aurobindo Pharma LimitedNDC
65862040560
Classification
Generic
Dosage Form
TABLET
Route
ORAL
Last Updated
2/22/2017
Active Ingredients
VENLAFAXINE HYDROCHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA090555On Market Since
4/7/2010
Pharmacological Classes
Norepinephrine Uptake Inhibitors
Serotonin Uptake Inhibitors
Serotonin and Norepinephrine Reuptake Inhibitor
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