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
- 0781-5439_5da86042-4c5d-4778-9125-19c942e112e5
- Product NDC
- 0781-5439
- Form
- TABLET, FILM COATED
- Composition / generic term
- Cefpodoxime Proxetil
- Labeler
- Sandoz Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20080528
- Source listing expiry
- 20271231
Source-listed ingredients
- CEFPODOXIME PROXETIL — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (0781-5439-01) · 0781-5439-01
- 20 TABLET, FILM COATED in 1 BOTTLE (0781-5439-20) · 0781-5439-20
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 →