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Clinical data | |
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Trade names | Fraxiparin(e), Fraxodi, others |
AHFS/ Drugs.com | International Drug Names |
Routes of administration | Subcutaneous injection (except for haemodialysis) |
ATC code | |
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Pharmacokinetic data | |
Bioavailability | 89% (SC dose) |
Elimination half-life | 3.7 hours (SC dose) |
Excretion | clearance 21.4mL/min (+/- 7) |
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CompTox Dashboard ( EPA) | |
ECHA InfoCard | 100.029.698 |
Chemical and physical data | |
Molar mass | 4300 g/mol |
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Nadroparin (trade names Fraxiparin[e], Fraxodi, among others) is an anticoagulant belonging to a class of drugs called low molecular weight heparins (LMWHs). Nadroparin was developed by Sanofi-Synthélabo.
Nadroparin is used in general and orthopedic surgery to prevent thromboembolic disorders ( deep vein thrombosis and pulmonary embolism), and as treatment for deep vein thrombosis. It is also used to prevent clotting during hemodialysis, and for treatment of unstable angina and non-Q wave myocardial infarction. [1]
For the treatment and prevention of DVT, the drug is administered as a subcutaneous injection (under the skin), usually around the abdomen. It is on the World Health Organization's List of Essential Medicines. [2]