Venlafaxine Hydrochloride 50771-0003
Product NDC
50771-0003- Manufacturer
- Yaopharma Co., Ltd.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 6, 2016
- Listing Expires
- December 31, 2026
- Application
- ANDA202036
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Venlafaxine Hydrochloride | 50 mg/1 |
Drug Class
Norepinephrine Uptake Inhibitors [MoA]Serotonin Uptake Inhibitors [MoA]Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
Packaging Options(1)
100 TABLET in 1 BOTTLE, PLASTIC (50771-003-02)