NDC 61919-480
Citalopram Hydrobromide 40 mg tablet
On the label: Direct Rx. It's repackaged: Direct Rx rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 57664-509.
Where the pills inside were 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 |
Repackaging site
- Direct Rx, Dawsonville, GA, United States · repackages it and relabels it
Product details
- Generic drug
- Citalopram: every company that makes it
- Form
- tablet
- Strength
- 40 mg
- Approval
- ANDA ANDA077032
- On the market since
- Jan 1, 2014
- Package NDCs
61919-480-30- Official label
- DailyMed (National Library of Medicine), updated Jan 22, 2020
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