United States· US:31722-843_3de3bb2e-97bf-4a59-e063-6294a90a7744

ELTROMBOPAG

A other systemic hemostatics product containing eltrombopag, registered in United States by Camber Pharmaceuticals, Inc.. The same ATC class is registered in 3 of our 19 countries.

ATC B02BXOrange BookUS 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…normalisedELTROMBOPAGATCB02BXREGISTER NO.US:31722-843_3de3bb2e…PACKS LISTED2CHECKEDSeptember 12, 2026

Where it is registered

Eltrombopag is registered in 3 of 19 countries.

Countries holding a registration under ATC B02BX (other systemic hemostatics), each read from that country’s own register.

  • This record: United States, from FDA National Drug Code directory (United States)
  • 3 of them publish a price we can compare per daily dose

Eltrombopag · ATC B02BX

3 / 19 countries

  • Polandprice
  • Switzerlandprice
  • United Statesprice
Blue: a registration under this ATC code. The ringed marker is this record’s country. Markets marked price publish a price we can compare per daily dose.

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
ELTROMBOPAG
Manufacturer
Camber Pharmaceuticals, Inc.
Country
United States (US)
ATC code
B02BX
ATC class
Other systemic hemostatics
Reimbursed
Not published by this register
Source register
FDA National Drug Code directory (United States)
Last checked
September 12, 2026

Packs & prices · 2

  • ndc11
    3172284330
    30 TABLET, FILM COATED in 1 BOTTLE (31722-843-30)
  • ndc11
    3172284314
    14 TABLET, FILM COATED in 1 BOTTLE (31722-843-14)

Regulatory notes

UNII (FDA substance ID)
4U07F515LG
ELTROMBOPAG OLAMINE
RxCUI 735651
Orange Book
A206788
ABABABAB
DailyMed SPL labels
1 version tracked

Same medicine, other countries

Eltrombopag in 11 other countries

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

All eltrombopag products

Authorised across Europe · EMA

The same active substance is authorised in 30 EEA countries. Names it is sold under:

  • Austria · Elrevolan, Eltrombopag +pharma
  • Belgium · Eltrombopag Krka
  • Bulgaria · Eltrombopag Pharmascience, Eltrombopag Pharmdedict
  • Cyprus · Eltrombopag Msn, Eltrombopag Sandoz
  • Czechia · Eltrombopag Abdi, Eltrombopag Krka
  • Germany · Eltrombopag 1 A Pharma, Eltrombopag Abdi
  • Denmark · Eltrombopag Glenmark, Eltrombopag Krka
  • Estonia · Eltrombopag Krka, Eltrombopag Msn
  • Spain · Eltrombgopa Glenmark, Eltrombopag Aurovitas Spain
  • Finland · Eltrombopag Avansor, Eltrombopag Krka
  • France · Eltrombopag Biogaran, Eltrombopag Eg
  • United Kingdom (Northern Ireland) · Eltrombopag Abdi, Eltrombopag Accord
  • Greece · Eltrombopag Anabiosis, Eltrombopag Faran
  • Croatia · Eltrombopag Alpha-Medical, Eltrombopag Msn
  • Hungary · Elrevolan, Eltrombopag Elpen
  • Ireland · Eltrombopag Clonmel, Eltrombopag Krka
  • Iceland · Eltrombopag Accord, Eltrombopag Coripharma
  • Italy · Elrevolan, Eltrombopag Abdi
  • Liechtenstein · Eltrombopag Accord, Eltrombopag Viatris
  • Lithuania · Eltrombopag Krka, Eltrombopag Msn
  • Latvia · Eltrombopag Krka, Eltrombopag Olpha
  • Malta · Eltrombopag Aspen, Eltrombopag Clonmel
  • Netherlands · Eltrombopag Abdi, Eltrombopag Amarox
  • Norway · Eltrombopag Accord, Eltrombopag Glenmark
  • Poland · Eltrombopag Glenmark, Eltrombopag Krka
  • Portugal · Eltrombopag Bluepharma, Eltrombopag Cipla
  • Romania · Eltrombopag Dr. Reddy’s, Eltrombopag Msn
  • Sweden · Eltrombopag Anabiosis, Eltrombopag Avansor
  • Slovenia · Eltrombopag Krka, Eltrombopag Msn
  • Slovakia · Eltrombopag Glenmark, Eltrombopag Krka

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/b9c342a4-d6aa-44a9-a0bd-73a733b238a0
GET /v1/drugs/b9c342a4-d6aa-44a9-a0bd-73a733b238a0?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.

{
  "unii": {
    "unii": "4U07F515LG",
    "rxcui": "735651",
    "inchikey": "PLILLUUXAVKBPY-SBIAVEDLSA-N",
    "display_name": "ELTROMBOPAG OLAMINE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "livertox": {
    "summary": null,
    "livertox_id": null,
    "hepatotoxicity_score": 5
  },
  "spl_meta": {
    "4af8f855-f710-e96f-e063-6294a90abb46": {
      "match": "brand_token",
      "title": "ELTROMBOPAG OLAMINE (ELTROMBOPAG) TABLET, FILM COATED [AVKARE]",
      "spl_version": "2",
      "published_date": "2026-05-22"
    }
  },
  "productid": "31722-843_3de3bb2e-97bf-4a59-e063-6294a90a7744",
  "productndc": "31722-843",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "206788",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 12.5MG ACID",
        "product_no": "001",
        "approval_date": "Jan 17, 2025"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 25MG ACID",
        "product_no": "002",
        "approval_date": "Jan 17, 2025"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 50MG ACID",
        "product_no": "003",
        "approval_date": "Jan 17, 2025"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 75MG ACID",
        "product_no": "004",
        "approval_date": "Jan 17, 2025"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "ELTROMBOPAG OLAMINE",
  "proprietary_name": "ELTROMBOPAG",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA206788",
  "marketing_category": "ANDA",
  "nonproprietary_name": "ELTROMBOPAG",
  "start_marketing_date": "20250513",
  "active_numerator_strength": "50"
}

See everything about eltrombopag.

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.