Fluoxetine Hydrochloride 51672-5306
Product NDC
51672-5306- Manufacturer
- Taro Pharmaceuticals U.s.a., Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 15, 2019
- Listing Expires
- December 31, 2026
- Application
- ANDA211477
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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(2)
500 TABLET, FILM COATED in 1 BOTTLE (51672-5306-2)
30 TABLET, FILM COATED in 1 BOTTLE (51672-5306-6)