Fluoxetine Hydrochloride 43598-0632
Product NDC
43598-0632- Manufacturer
- Dr. Reddy's Laboratories Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 28, 2019
- Listing Expires
- December 31, 2026
- Application
- ANDA211721
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Fluoxetine Hydrochloride | 60 mg/1 |
Drug Class
Serotonin Reuptake Inhibitor [EPC]Serotonin Uptake Inhibitors [MoA]
Packaging Options(2)
100 TABLET, FILM COATED in 1 BOTTLE (43598-632-01)
30 TABLET, FILM COATED in 1 BOTTLE (43598-632-30)