Fluoxetine 42571-0388
Product NDC
42571-0388- Manufacturer
- Micro Labs Limited
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 1, 2023
- Listing Expires
- December 31, 2026
- Application
- ANDA216232
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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(3)
100 CAPSULE in 1 BOTTLE (42571-388-01)
1000 CAPSULE in 1 BOTTLE (42571-388-10)
30 CAPSULE in 1 BOTTLE (42571-388-30)