NDC 51662-1532
Tranexamic Acid 100 mg per 1 mL injection, solution
On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged: HF Acquisition Co. LLC. DBA HealthFirst rebottles it from AuroMedics Pharma LLC's NDC 55150-188.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Eugia Pharma Specialities Limited | Sangareddy, India | Makes it, tests it and packages it | Serious problems, FDA actionFeb 6, 2026 · 7 inspections, 2 with FDA action |
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Recalls
- Sep 26, 2022 · Class III · AuroMedics Pharma LLC
Presence of Particulate Matter: Piece of metal found in a vial
Lots: Lot: CTA210006, Exp. 02/2024
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Tranexamic Acid: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 100 mg per 1 mL
- Approval
- ANDA ANDA205035
- On the market since
- Jun 20, 2021
- Package NDCs
51662-1532-151662-1532-251662-1532-3- Official label
- DailyMed (National Library of Medicine), updated Jan 30, 2024
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