NDC 64725-0507
citalopram hydrobromide 10 mg tablet
On the label: TYA Pharmaceuticals. It's repackaged: TYA Pharmaceuticals rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 57664-507.
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
- TYA Pharmaceuticals, Location not on file · repackages it and relabels it
Product details
- Generic drug
- Citalopram: every company that makes it
- Form
- tablet
- Strength
- 10 mg
- Approval
- ANDA ANDA077032
- On the market since
- Nov 12, 2004
- Package NDCs
64725-0507-1- Official label
- DailyMed (National Library of Medicine), updated Jan 31, 2013
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