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
69043-006_36f0759f-b50b-4a49-869b-d73f5ad7d8cf
Product NDC
69043-006
Form
TABLET, FILM COATED
Composition / generic term
CEFPODOXIME PROXETIL
Labeler
Cronus Pharma LLC
Marketing category
ANDA
Marketing start / end (source format)
20070611
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 (69043-006-01) · 69043-006-01
  • 250 TABLET, FILM COATED in 1 BOTTLE (69043-006-25) · 69043-006-25

Source and coverage

Open FDA National Drug Code directory

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.

Browse United States records →