Fluoxetine 49884-0468
Product NDC
49884-0468- Manufacturer
- Endo Usa, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 16, 2017
- Listing Expires
- December 31, 2026
- Application
- ANDA209419
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Fluoxetine Hydrochloride | 60 mg/1 |
Drug Class
Serotonin Reuptake Inhibitor [EPC]Serotonin Uptake Inhibitors [MoA]
Packaging Options(1)
30 TABLET, FILM COATED in 1 BOTTLE (49884-468-11)