Friday, July 10, 2026

Drug profile · INN

cefixime

cefixime (SUPRAX) is a bacterial penicillin-binding protein inhibitor. Route of administration: oral. Current US regulatory status: approved.

FDA: approved
US status approved
Patents linked 0
Pipeline programs 2
News articles 0
Drug details — cefixime
US status
approved
Class
Route
ORAL
Patents
0
Programs
2
Data quality
0.84

Quick answer

cefixime (SUPRAX) is a bacterial penicillin-binding protein inhibitor. Route of administration: oral. Current US regulatory status: approved.

Key facts

INN cefixime
Brand SUPRAX
Mechanism Bacterial penicillin-binding protein inhibitor
Target Bacterial penicillin-binding protein
Route ORAL
Formulation FOR SUSPENSION

Mechanism of action

Bacterial penicillin-binding protein inhibitor

Primary target: Bacterial penicillin-binding protein

Approval history

Authority Status Date
FDA approved

Pipeline programs

  1. APHP211043 Phase 3 · PARItec · acute pyelonephritis (AP) in children
  2. CEFOSPROST Approved · George Institute for · Acute bacterial prostatitis

Related & competitor drugs

  1. amoxicillin Bacterial penicillin-binding protein inhibitor
  2. ampicillin sodium Bacterial penicillin-binding protein inhibitor
  3. ampicillin/ampicillin trihydrate Bacterial penicillin-binding protein inhibitor
  4. cefaclor Bacterial penicillin-binding protein inhibitor
  5. cefadroxil/cefadroxil hemihydrate Bacterial penicillin-binding protein inhibitor
  6. cefazolin sodium Bacterial penicillin-binding protein inhibitor

Frequently asked questions

What is cefixime?

cefixime (SUPRAX) is a bacterial penicillin-binding protein inhibitor. Route of administration: oral. Current US regulatory status: approved.

What is the brand name for cefixime?

SUPRAX is a marketed brand name for cefixime. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of cefixime?

cefixime has approved status in the United States according to our Drugs@FDA-derived records. Verify on the official FDA label before clinical or commercial decisions.