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United States· US:69043-006_36f0759f-b50b-4a49-869b-d73f5ad7d8cf

CEFPODOXIME PROXETIL

A medicinal product containing cefpodoxime proxetil, registered in United States by Cronus Pharma LLC.

US label

Checked against FDA National Drug Code directory (United States) on

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedCEFPODOXIME PROXETILATC—REGISTER NO.US:69043-006_36f0759f…PACKS LISTED4CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
CEFPODOXIME PROXETIL
Manufacturer
Cronus Pharma LLC
Country
United States (US)
ATC code
—
Reimbursed
Not published by this register
Source register
FDA National Drug Code directory (United States)
Last checked
September 27, 2026

Packs & prices · 4

  • ndc11
    6904300601
    100 TABLET, FILM COATED in 1 BOTTLE (69043-006-01)
  • ndc11
    6904300625
    250 TABLET, FILM COATED in 1 BOTTLE (69043-006-25)
  • ndc11
    69043-006-01
  • ndc11
    69043-006-25

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Same medicine, other countries

Cefpodoxime proxetil in 4 other countries

What each register calls a product with the same active substance — salts and hydrates count as the same.

All cefpodoxime proxetil products

Authorised across Europe · EMA

The same active substance is authorised in 5 EEA countries. Names it is sold under:

  • Bulgaria · Сефпотек
  • Germany · Cefpo, Cefpodoxim Ratiopharm
  • France · Cefpodoxime Arrow Lab, Cefpodoxime Enfants Et Nourrissons Teva
  • Greece · Orebus
  • Italy · Cefodox, Cefodox Bambini

Source: European Medicines Agency, Article 57 product data.

Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of FDA National Drug Code directory (United States). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.

For developers

The same record over the API, and the raw payload
GET /v1/drugs/e525f92f-fa18-4ddb-a0eb-f701a99eb2a4
GET /v1/drugs/e525f92f-fa18-4ddb-a0eb-f701a99eb2a4?format=fhir

Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.

{
  "route": "ORAL",
  "source": "ndc",
  "strength": "100",
  "substance": "CEFPODOXIME PROXETIL",
  "productndc": "69043-006",
  "dosage_form": "TABLET, FILM COATED",
  "dea_schedule": null,
  "strength_unit": "mg/1",
  "application_number": "ANDA065370",
  "marketing_category": "ANDA"
}

See everything about cefpodoxime proxetil.

This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.