Venlafaxine Hydrochloride 82009-0056
Product NDC
82009-0056- Manufacturer
- Quallent Pharmaceuticals Health Llc
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 21, 2022
- Listing Expires
- December 31, 2026
- Application
- ANDA200834
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Venlafaxine Hydrochloride | 37.5 mg/1 |
Drug Class
Norepinephrine Uptake Inhibitors [MoA]Serotonin Uptake Inhibitors [MoA]Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
Packaging Options(1)
1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (82009-056-10)