Fluoxetine Hydrochloride 49884-0335
Product NDC
49884-0335- Manufacturer
- Endo Usa, Inc.
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 22, 2016
- Listing Expires
- December 31, 2026
- Application
- ANDA203836
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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(2)
100 TABLET, COATED in 1 BOTTLE, PLASTIC (49884-335-01)
30 TABLET, COATED in 1 BOTTLE, PLASTIC (49884-335-11)