Fluoxetine 71656-0089
Product NDC
71656-0089- Manufacturer
- Saptalis Pharmaceuticals, Llc.
- Dosage Form
- Solution
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 20, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA075525
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Fluoxetine Hydrochloride | 20 mg/5mL |
Drug Class
Serotonin Reuptake Inhibitor [EPC]Serotonin Uptake Inhibitors [MoA]
Packaging Options(1)
120 mL in 1 BOTTLE (71656-089-04)