Carbinoxamine
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Clinical data | |
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AHFS/Drugs.com | Monograph |
MedlinePlus | a606008 |
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Routes of administration |
Oral: 4 mg tablet or 4 mg/5 mL liquid |
ATC code | R06AA08 (WHO) |
Legal status | |
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Pharmacokinetic data | |
Biological half-life | 10 to 20 hours |
Identifiers | |
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CAS Number | 486-16-8 ![]() |
PubChem (CID) | 2564 |
IUPHAR/BPS | 7139 |
DrugBank | DB00748 ![]() |
ChemSpider | 2466 ![]() |
UNII | VED9E376NC ![]() |
KEGG | D07617 ![]() |
ChEBI | CHEBI:3398 ![]() |
ChEMBL | CHEMBL864 ![]() |
ECHA InfoCard | 100.006.935 |
Chemical and physical data | |
Formula | C16H19ClN2O |
Molar mass | 290.788 g/mol |
3D model (Jmol) | Interactive image |
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Carbinoxamine (Clistin, Palgic, Rondec, Rhinopront) is a antihistamine and anticholinergic agent. It was first launched in the United States by the McNeil Corporation under the brand name Clistin. It is now available under the brand name Palgic as 4 mg tablets or 4 mg/5 mL liquid. It is approved by the U.S. Food and Drug Administration (FDA) (specifically at the 4 mg dose/strength) for hay fever (a.k.a. allergic rhinitis, SAR and PAR); vasomotor rhinitis; mild urticaria; angioedema, dermatographism and allergic conjunctivitis. Carbinoxamine is a histamine antagonist, specifically an H1-antagonist. The maleic acid salt of the levorotatory isomer is sold as the prescription drug rotoxamine.
Carbinoxamine is available in various countries around the world by itself, combined with decongestants such as pseudoephedrine, and also with other ingredients including paracetamol, aspirin, and codeine.
In June 2006 the FDA announced that more than 120 branded pharmacy products containing carbinoxamine were being illegally marketed and demanded they be removed from the marketplace. This action was precipitated by twenty-one reported deaths in children under the age of two who had been administered carbinoxamine-containing products. Despite the fact that the drug had not been studied in this age group, a multitude of OTC preparations containing carbinoxamine were being marketed for infants and toddlers. At present, all carbinoxamine-containing formulations are approved only for adults or children ages 3 or older.[1]
Carbinoxamine is used in the treatment of severe itching in patients with CD5.[clarification needed]
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