NDC 55150-230
Fondaparinux Sodium 2.5 mg per 0.5 mL injection, solution
On the label: AuroMedics Pharma LLC.
Where it's 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 |
Recalls
- Sep 30, 2022 · Class II · AuroMedics Pharma LLC
Subpotent Drug: Out of specification for assay
Lots: Lot # CFN200020, EXP Nov. 2022
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Fondaparinux: every company that makes it
- Form
- injection, solution, subcutaneous
- Strength
- 2.5 mg per 0.5 mL
- Approval
- ANDA ANDA206918
- On the market since
- Dec 26, 2017
- Package NDCs
55150-230-0055150-230-0255150-230-10- Official label
- DailyMed (National Library of Medicine), updated Jan 10, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?