NDC 70518-4239
escitalopram 20 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Rising Pharma Holdings, Inc.'s NDC 16571-757.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Graviti Pharmaceuticals Private Limited | Sangareddy, India | Makes it and tests it | Problems found, fixed voluntarilyJul 28, 2026 · 2 inspections |
Product details
- Generic drug
- Escitalopram: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA078777
- On the market since
- Dec 13, 2024
- Package NDCs
70518-4239-070518-4239-170518-4239-270518-4239-3- Official label
- DailyMed (National Library of Medicine), updated Oct 23, 2026
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