UFIS-SWE-IG
0.1.0 - ci-build

UFIS-SWE-IG, published by UNICOM. This guide is not an authorized publication; it is the continuous build for version 0.1.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/joofio/ufis-swe-ig/ and changes regularly. See the Directory of published versions

Example Bundle: Nobligan100mgmloraladropparlos-SE-PLC-MPD-BBDL

Nobligan 100 mg/ml orala droppar, lösning

MPID: SE-100000515-00014305
EURDID: 3002

Full name: Nobligan 100 mg/ml orala droppar, lösning

- Invented name part: Nobligan

- Strength part: 100 mg/ml

- Pharmaceutical dose form part: orala droppar, lösning

Name usage: Swedish (Kingdom of Sweden)

Authorised dose form: Oral drops, solution

Legal status of supply: Medicinal product subject to medical prescription

Domain: Human use

Resource status: Current

Product classification:

  • 100000097261 tramadol

Marketing Authorisation 1 of 1

Authorisation number: 14305

Region: Kingdom of Sweden

Marketing authorisation holder: Grünenthal GmbH

Identifier:

  • LOC-100006949

Status: Valid (1998-11-20)

Package 1 of 1

PCID:

Description:
Flaska, 96 ml (glas)

Marketing status:

  • Kingdom of Sweden: Marketed

Pack size:

  • 1 Bottle

Package: 1 Box (Cardboard)

Containing:

Package: 1 Bottle (Glass)

Containing: 96 millilitre(s)

Manufactured Item

Dose form: Oral drops, solution

Unit of presentation: Bottle

Ingredient

Role: Active

Substance: Tramadol hydrochloride

Concentration strength: 100 milligram(s) / 1 millilitre(s)

Reference strength:
Tramadol 88 milligram(s) / 1 millilitre(s)

Administrable Product (1 of 1)

Dose form: Oral drops, solution

Unit of presentation:

Route of administration:

  • Oral use

Ingredients:

Ingredient

Role: Active

Substance: Tramadol hydrochloride

Concentration strength: 100 milligram(s) / 1 millilitre(s)

Reference strength:
Tramadol 88 milligram(s) / 1 millilitre(s)