Fluoxetine Hydrochloride 68180-0998
Product NDC
68180-0998- Manufacturer
- Lupin Pharmaceuticals, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 7, 2019
- Listing Expires
- December 31, 2026
- Application
- ANDA211653
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Fluoxetine Hydrochloride | 10 mg/1 |
Drug Class
Serotonin Reuptake Inhibitor [EPC]Serotonin Uptake Inhibitors [MoA]
Packaging Options(2)
100 TABLET in 1 BOTTLE (68180-998-01)
30 TABLET in 1 BOTTLE (68180-998-06)