United States · FDA National Drug Code directory

Cefpodoxime Proxetil

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
69292-514_157c18ee-7809-4e05-8caa-0359ef50142e
Product NDC
69292-514
Form
TABLET, FILM COATED
Composition / generic term
Cefpodoxime Proxetil
Labeler
Amici Pharmaceuticals, LLC.
Marketing category
ANDA
Marketing start / end (source format)
20221221
Source listing expiry
20261231

Source-listed ingredients

  • CEFPODOXIME PROXETIL — 100 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET, FILM COATED in 1 BOTTLE (69292-514-01) · 69292-514-01
  • 500 TABLET, FILM COATED in 1 BOTTLE (69292-514-50) · 69292-514-50

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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