Fluoxetine 51655-0100
Generic: Fluoxetine Hydrochloride
Product NDC
51655-0100- Manufacturer
- Northwind Health Company, Llc
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 20, 2014
- Listing Expires
- December 31, 2027
- Application
- ANDA078619
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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)
90 CAPSULE in 1 BOTTLE, PLASTIC (51655-100-26)
30 CAPSULE in 1 BOTTLE, DISPENSING (51655-100-52)