Fluoxetine 72603-0489
Product NDC
72603-0489- Manufacturer
- Northstar Rx Llc
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 1, 2025
- 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(2)
100 CAPSULE in 1 BOTTLE (72603-489-01)
1000 CAPSULE in 1 BOTTLE (72603-489-02)