United States · FDA National Drug Code directory

Cefuroxime axetil

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
43063-657_4139efd1-921a-b349-e063-6394a90a0404
Product NDC
43063-657
Form
TABLET, FILM COATED
Composition / generic term
Cefuroxime axetil
Labeler
PD-Rx Pharmaceuticals, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20101201
Source listing expiry
20261231

Source-listed ingredients

  • CEFUROXIME AXETIL — 250 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-657-20) · 43063-657-20
  • 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-657-60) · 43063-657-60

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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