NDC 57664-508
citalopram hydrobromide 20 mg tablet
On the label: Caraco Pharmaceutical Laboratories, Ltd..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sun Pharmaceutical Industries Limited | Halol, India | Makes it | Serious problems, FDA actionJun 13, 2025 · 12 inspections, 5 with FDA action |
Product details
- Generic drug
- Citalopram: every company that makes it
- Form
- tablet
- Strength
- 20 mg
- Approval
- ANDA ANDA077032
- On the market since
- May 29, 2015
- Package NDCs
57664-508-1357664-508-1857664-508-88- Official label
- DailyMed (National Library of Medicine), updated Dec 7, 2022
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