Escitalopram Oxalate 16571-0769
Product NDC
16571-0769- Manufacturer
- Rising Pharma Holdings, Inc.
- Dosage Form
- Solution
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 3, 2012
- Listing Expires
- December 31, 2027
- Application
- ANDA079062
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Escitalopram Oxalate | 5 mg/5mL |
Drug Class
Serotonin Reuptake Inhibitor [EPC]Serotonin Uptake Inhibitors [MoA]
Packaging Options(1)
240 mL in 1 BOTTLE (16571-769-24)