Escitalopram Oxalate 65162-0021
Product NDC
65162-0021- Manufacturer
- Amneal Pharmaceuticals Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 17, 2017
- Listing Expires
- December 31, 2026
- Application
- ANDA205619
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Escitalopram Oxalate | 20 mg/1 |
Drug Class
Serotonin Reuptake Inhibitor [EPC]Serotonin Uptake Inhibitors [MoA]
Packaging Options(4)
30 TABLET, FILM COATED in 1 BOTTLE (65162-021-03)
90 TABLET, FILM COATED in 1 BOTTLE (65162-021-09)
1000 TABLET, FILM COATED in 1 BOTTLE (65162-021-11)
500 TABLET, FILM COATED in 1 BOTTLE (65162-021-50)