Fluoxetine 82009-0101
Generic: Fluoxetine Hydrochloride
Product NDC
82009-0101- Manufacturer
- Quallent Pharmaceuticals Health Llc
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 1, 2023
- Listing Expires
- December 31, 2026
- Application
- ANDA078619
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Fluoxetine Hydrochloride | 20 mg/1 |
Drug Class
Serotonin Reuptake Inhibitor [EPC]Serotonin Uptake Inhibitors [MoA]
Packaging Options(1)
1000 CAPSULE in 1 BOTTLE (82009-101-10)