NDC 53808-0922
citalopram hydrobromide 40 mg tablet
On the label: State of Florida DOH Central Pharmacy. It's repackaged: State of Florida DOH Central Pharmacy 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
- State of Florida DOH Central Pharmacy, Location not on file · repackages 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
53808-0922-1- Official label
- DailyMed (National Library of Medicine), updated Sep 30, 2014
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