Venlafaxine 57237-0172
Generic: Venlafaxine Hydrochloride
Product NDC
57237-0172- Manufacturer
- Rising Pharma Holdings, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 7, 2010
- Listing Expires
- December 31, 2026
- Application
- ANDA090555
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Venlafaxine Hydrochloride | 25 mg/1 |
Drug Class
Norepinephrine Uptake Inhibitors [MoA]Serotonin Uptake Inhibitors [MoA]Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
Packaging Options(2)
100 TABLET in 1 BOTTLE (57237-172-01)
90 TABLET in 1 BOTTLE (57237-172-90)