Lornoxicam
| Clinical data | |
|---|---|
| Trade names | Xefo, Xefocam others |
| AHFS/Drugs.com | International Drug Names |
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| Routes of administration | By mouth, parenteral |
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| Pharmacokinetic data | |
| Bioavailability | 90–100% |
| Protein binding | 99% |
| Metabolism | CYP2C9 |
| Elimination half-life | 3–4 hours |
| Excretion | 2/3 liver, 1/3 kidney |
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| CompTox Dashboard (EPA) | |
| ECHA InfoCard | 100.158.646 |
| Chemical and physical data | |
| Formula | C13H10ClN3O4S2 |
| Molar mass | 371.81 g·mol−1 |
| 3D model (JSmol) | |
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| (what is this?) (verify) | |
Lornoxicam, also known as chlortenoxicam, is a nonsteroidal anti-inflammatory drug (NSAID) of the oxicam class with analgesic (pain relieving), anti-inflammatory and antipyretic (fever reducing) properties. It is available in oral and parenteral formulations.
It was patented in 1977 and approved for medical use in 1997. Brand names include Xefo and Xefocam among others.