Escitalopram Oxalate 82009-0037
Product NDC
82009-0037- Manufacturer
- Quallent Pharmaceuticals Health Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 1, 2023
- Listing Expires
- December 31, 2026
- Application
- ANDA090939
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Escitalopram Oxalate | 20 mg/1 |
Drug Class
Serotonin Reuptake Inhibitor [EPC]Serotonin Uptake Inhibitors [MoA]
Packaging Options(1)
1000 TABLET in 1 BOTTLE (82009-037-10)