Fluoxetine 42708-0200
Product NDC
42708-0200- Manufacturer
- Qpharma Inc
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 11, 2025
- Listing Expires
- December 31, 2027
- 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)
30 CAPSULE in 1 BOTTLE, PLASTIC (42708-200-30)