Venlafaxine Hydrochloride 63629-2100
Product NDC
63629-2100- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 31, 2019
- Listing Expires
- December 31, 2026
- Application
- ANDA209193
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Venlafaxine Hydrochloride | 150 mg/1 |
Drug Class
Norepinephrine Uptake Inhibitors [MoA]Serotonin Uptake Inhibitors [MoA]Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
Packaging Options(1)
30 TABLET in 1 BOTTLE (63629-2100-1)