Venlafaxine 46708-0432
Product NDC
46708-0432- Manufacturer
- Alembic Pharmaceuticals Limited
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 1, 2015
- Listing Expires
- December 31, 2026
- Application
- ANDA078932
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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(3)
30 TABLET in 1 BOTTLE (46708-432-30)
100 TABLET in 1 BOTTLE (46708-432-31)
1000 TABLET in 1 BOTTLE (46708-432-91)