United States· US:64980-402_803b37ff-46c6-4dcb-9d9f-a118c4c4601b
Cefpodoxime Proxetil
A medicinal product containing cefpodoxime proxetil, registered in United States by Rising Pharma Holdings, Inc..
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- CEFPODOXIME PROXETIL
- Manufacturer
- Rising Pharma Holdings, 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 · 4
- ndc1164980402101 BOTTLE in 1 CARTON (64980-402-10) / 100 mL in 1 BOTTLE
- ndc1164980402501 BOTTLE in 1 CARTON (64980-402-50) / 50 mL in 1 BOTTLE
- ndc1164980-402-10
- ndc1164980-402-50
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.
- FranceCEFPODOXIME ARROW ENFANTS ET NOURRISSONS 40 mg/5 ml, poudre pour suspension buvableARROW GENERIQUES
- FinlandCefpobactHexal AG
- CzechiaFOREXOAlkaloid - INT d.o.o., Ljubljana - Črnuče
- GermanyCefpoBasics Gmbh
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/d90e1b28-ef56-431c-b7c6-55072efdb045 GET /v1/drugs/d90e1b28-ef56-431c-b7c6-55072efdb045?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": "50",
"substance": "CEFPODOXIME PROXETIL",
"productndc": "64980-402",
"dosage_form": "GRANULE, FOR SUSPENSION",
"dea_schedule": null,
"strength_unit": "mg/5mL",
"application_number": "ANDA065409",
"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.