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United States· US:70518-4676_5372f543-8c7e-8a8a-e063-6394a90a078b

Cefpodoxime Proxetil

A medicinal product containing cefpodoxime proxetil, registered in United States by REMEDYREPACK INC..

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:70518-4676_5372f54…PACKS LISTED1CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
CEFPODOXIME PROXETIL
Manufacturer
REMEDYREPACK INC.
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 · 1

  • ndc11
    70518-4676-0

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/dc0d1b3d-8892-4da9-8ce2-6cb92d0f6449
GET /v1/drugs/dc0d1b3d-8892-4da9-8ce2-6cb92d0f6449?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": "200",
  "substance": "CEFPODOXIME PROXETIL",
  "productndc": "70518-4676",
  "dosage_form": "TABLET, FILM COATED",
  "dea_schedule": null,
  "strength_unit": "mg/1",
  "application_number": "ANDA210568",
  "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.