Escitalopram 68788-8569
Product NDC
68788-8569- Manufacturer
- Preferred Pharmaceuticals Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 23, 2024
- Listing Expires
- December 31, 2027
- Application
- ANDA078777
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Escitalopram Oxalate | 10 mg/1 |
Drug Class
Serotonin Reuptake Inhibitor [EPC]Serotonin Uptake Inhibitors [MoA]
Packaging Options(4)
100 TABLET, FILM COATED in 1 BOTTLE (68788-8569-1)
30 TABLET, FILM COATED in 1 BOTTLE (68788-8569-3)
60 TABLET, FILM COATED in 1 BOTTLE (68788-8569-6)
90 TABLET, FILM COATED in 1 BOTTLE (68788-8569-9)