Cefoxitin

DB01331ApprovedInvestigationalSmall moleculeCephalosporins

Cefoxitin is a semi-synthetic, broad-spectrum antibiotic for parenteral administration used for the treatment of serious bacterial infections, such as urinary tract infection, blood infection, bone and joint infection, and lower respiratory tract infection. It is derived from cephamycin C, which is produced by Streptomyces lactamdurans.

Chemical structure of Cefoxitin
Mechanism
Curator reviewed
Primary indication
For the treatment of serious infections caused by susceptible strains microorganisms.Curator reviewed · 18 structured indications
Formula / weight
C16H17N3O7S2 · 427.452 g/mol (avg)
First approval
Canada, 2013 · United States, 1978
Also known as
Ceftoxitin · Cephoxitin · Rephoxitin
Code names
J01DC01

Resolves to

Structure
InChIKeyWZOZEZRFJCJXNZ-ZBFHGGJFSA-NSMILES[H][C@]12SCC(COC(N)=O)=C(N1C(=O)[C@]2(NC(=O)CC1=CC=CS1)OC)C(O)=O

What you can answer from here — as of September 23, 2026

13Protein targetsEach mapped to UniProt, with action and pharmacological action
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804Drug interactionsStructured to mechanism, not free text
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15Clinical trialsPhase, status and sponsor resolved per trial
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18Structured indicationsCondition, population, route and combination as fields, not prose
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57Marketed productsAcross 4 countries and 17 labellers
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1ATC codeIncluding every combination product, plus 15 drug categories
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18+ReferencesStructured and connected to the statements they support
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Which drugs share a target with Cefoxitin, and which of those have an active Phase 3 trial?

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