Venlafaxine Hydrochloride 80425-0477
Product NDC
80425-0477- Manufacturer
- Advanced Rx Of Tennessee, Llc
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 30, 2025
- Listing Expires
- December 31, 2026
- Application
- NDA022104
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Venlafaxine Hydrochloride | 37.5 mg/1 |
Drug Class
Norepinephrine Uptake Inhibitors [MoA]Serotonin Uptake Inhibitors [MoA]Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
Packaging Options(3)
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0477-1)
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0477-2)
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0477-3)