Fluoxetine Hydrochloride 70954-0600
Product NDC
70954-0600- Manufacturer
- Ani Pharmaceuticals, Inc.
- Dosage Form
- Solution
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 9, 2022
- Listing Expires
- December 31, 2027
- Application
- ANDA216448
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Fluoxetine Hydrochloride | 20 mg/5mL |
Drug Class
Serotonin Reuptake Inhibitor [EPC]Serotonin Uptake Inhibitors [MoA]
Packaging Options(1)
120 mL in 1 BOTTLE, PLASTIC (70954-600-10)