Fluoxetine 50228-0421
Product NDC
50228-0421- Manufacturer
- Sciegen Pharmaceuticals, Inc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 20, 2019
- Listing Expires
- December 31, 2026
- Application
- ANDA210935
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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(3)
100 TABLET, FILM COATED in 1 BOTTLE (50228-421-01)
1000 TABLET, FILM COATED in 1 BOTTLE (50228-421-10)
30 TABLET, FILM COATED in 1 BOTTLE (50228-421-30)