Loxoprofen
| Clinical data | |
|---|---|
| AHFS/Drugs.com | International Drug Names |
| Routes of administration | Oral, transdermal |
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| Pharmacokinetic data | |
| Protein binding | 97% |
| Metabolism | Liver glucuronidation |
| Elimination half-life | 75 minutes |
| Excretion | Kidney |
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| Chemical and physical data | |
| Formula | C15H18O3 |
| Molar mass | 246.306 g·mol−1 |
| 3D model (JSmol) | |
| Chirality | Racemic mixture |
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| (what is this?) (verify) | |
Loxoprofen is a nonsteroidal anti-inflammatory drug (NSAID) in the propionic acid derivatives group, which also includes ibuprofen and naproxen among others. It is available in some countries for oral administration. A transdermal preparation was approved for sale in Japan in January 2006; medicated tape and gel formulations followed in 2008 and 2010.
It was patented in 1977 and approved for medical use in 1986.