Escitalopram 70518-4239
Product NDC
70518-4239- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 13, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA078777
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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 BLISTER PACK (70518-4239-0)
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4239-1)
7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4239-2)
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4239-3)