Fluoxetine 42708-0025
Product NDC
42708-0025- Manufacturer
- Qpharma Inc
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 29, 2002
- Listing Expires
- December 31, 2026
- Application
- ANDA076001
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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)
30 CAPSULE in 1 BOTTLE (42708-025-30)