Fluoxetine 55111-0150
Product NDC
55111-0150- Manufacturer
- Dr.reddy's Laboratories Limited
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 30, 2016
- Listing Expires
- December 31, 2026
- Application
- ANDA076006
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Fluoxetine Hydrochloride | 10 mg/1 |
Drug Class
Serotonin Reuptake Inhibitor [EPC]Serotonin Uptake Inhibitors [MoA]
Packaging Options(5)
100 TABLET, FILM COATED in 1 BOTTLE (55111-150-01)
500 TABLET, FILM COATED in 1 BOTTLE (55111-150-05)
1000 TABLET, FILM COATED in 1 BOTTLE (55111-150-10)
30 TABLET, FILM COATED in 1 BOTTLE (55111-150-30)
10 BLISTER PACK in 1 CARTON (55111-150-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-150-79)