Venlafaxine 70518-4500
Product NDC
70518-4500- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 12, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA214127
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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)
90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4500-0)