Fluoxetine 68645-0130
Product NDC
68645-0130- Manufacturer
- Legacy Pharmaceutical Packaging, Llc
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 25, 2011
- Listing Expires
- December 31, 2027
- Application
- ANDA076001
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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(1)
30 CAPSULE in 1 BOTTLE (68645-130-54)