Fluoxetine 59651-0309
Product NDC
59651-0309- Manufacturer
- Aurobindo Pharma Limited
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 8, 2020
- Listing Expires
- December 31, 2026
- Application
- ANDA213286
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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 TABLET, FILM COATED in 1 BOTTLE (59651-309-01)
30 TABLET, FILM COATED in 1 BOTTLE (59651-309-30)