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Belgium· BE-AMP-SAM112217-00

Bromhydrate de Scopolamine 0,50 mg/ml

A medicinal product containing hyoscine hydrobromide, registered in Belgium by Laboratoires Sterop.

Checked against FAMHP / AFMPS (Belgium) on

Informational only — not a medical device.

SOURCE REGISTER · BEFAMHP / AFMPS (Belgium)normalisedBromhydrate de Scopolamine 0,50 mg/mlATC—REGISTER NO.BE-AMP-SAM112217-00PACKS LISTED2CHECKEDSeptember 26, 2026

The record

At a glance

FAMHP / AFMPS (Belgium)
Active substance
Hyoscine Hydrobromide
Manufacturer
Laboratoires Sterop
Country
Belgium (BE)
ATC code
—
Reimbursed
Not published by this register
Source register
FAMHP / AFMPS (Belgium)
Last checked
September 26, 2026

Packs & prices · 2

  • be_apb
    1847995
  • be_apb
    1847979

Regulatory notes

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

Same medicine, other countries

Hyoscine hydrobromide in 14 other countries

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

All hyoscine hydrobromide products

Authorised across Europe · EMA

The same active substance is authorised in 13 EEA countries. Names it is sold under:

  • Germany · Boro-Scopol N, Scopoderm Tts
  • Denmark · Scopoderm
  • Spain · Escopolamina B. Braun
  • Finland · Scopoderm
  • France · Bromhydrate De Scopolamine Renaudin, Scopoderm Tts
  • United Kingdom (Northern Ireland) · Hyoscine Hydrobromide Wockhardt Uk, Hyoscine Martindale Pharma
  • Ireland · Hyoscine Injection Bp Ethypharm, Kwells
  • Iceland · Scopoderm
  • Luxembourg · Scopoderm Tts
  • Malta · Kwells
  • Netherlands · Scopoderm
  • Norway · Scopoderm
  • Sweden · Scopoderm

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 FAMHP / AFMPS (Belgium). 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/bbf5f47c-9d84-48ee-a78f-939fce03c726
GET /v1/drugs/bbf5f47c-9d84-48ee-a78f-939fce03c726?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.

{
  "form": "Solvent for parenteral use",
  "source": "afmps",
  "status": "REVOKED",
  "name_en": "Bromhydrate de Scopolamine 0,50 mg/ml",
  "name_fr": "Bromhydrate de Scopolamine 0,50 mg/ml",
  "name_nl": "Bromhydrate de Scopolamine 0,50 mg/ml",
  "amp_code": "SAM112217-00",
  "strengths": [
    "0.5000"
  ],
  "pack_count": 2,
  "substances": [
    "Hyoscine Hydrobromide"
  ],
  "medicine_type": "ALLOPATHIC",
  "atc_description": null,
  "authorisation_numbers": [
    "0301P 0034F012"
  ]
}

See everything about hyoscine hydrobromide.

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.