NDC 52959-773
Citalopram 20 mg tablet
On the label: H.J. Harkins Co., Inc.. It's repackaged: H.J. Harkins Co., Inc. rebottles it from Aurolife Pharma LLC's NDC 13107-006.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurolife Pharma LLC | Dayton, NJ, United States | Makes it | Serious problems, FDA actionDec 7, 2021 · 10 inspections, 1 with FDA action |
| Aurolife Pharma LLC | Dayton, NJ, United States | Packages it, labels it, repackages it and relabels it | Serious problems, FDA actionDec 7, 2021 · 10 inspections, 1 with FDA action |
Product details
- Generic drug
- Citalopram: every company that makes it
- Form
- tablet
- Strength
- 20 mg
- Approval
- ANDA ANDA077031
- On the market since
- Jan 1, 2009
- Package NDCs
52959-773-3052959-773-5252959-773-60- Official label
- DailyMed (National Library of Medicine), updated Nov 2, 2011
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