Venlafaxine Hydrochloride 00093-9149
Product NDC
00093-9149- Manufacturer
- Teva Pharmaceuticals Usa, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 4, 2006
- Listing Expires
- December 31, 2026
- Application
- ANDA076690
Need to source Venlafaxine Hydrochloride? Find it on a pharmacy-to-pharmacy marketplace at better prices.
✓ DSCSA Compliant. ✓ Verified Pharmacies Only.P2P pharmacy marketplace.
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 (0093-9149-01)