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: SimvastatinBluefish-20mg-Tablet-SE-BS-MPD-BBDL

Simvastatin Bluefish 20 mg filmdragerad tablett

MPID: SE-100002566-00026678
EURDID: 2709

Full name: Simvastatin Bluefish 20 mg filmdragerad tablett

- Scientific name part: SimvastatinBluefish

- Strength part: 20 mg

- Pharmaceutical dose form part: Filmdragerad tablett

Name usage: Swedish (Kingdom of Sweden)

Authorised dose form: Film-coated tablet

Legal status of supply: Medicinal product subject to medical prescription

Domain: Human use

Resource status: Current

Product classification:

  • 100000095169 simvastatin

Marketing Authorisation 1 of 1

Authorisation number: 26678

Region: Kingdom of Sweden

Marketing authorisation holder: Bluefish Pharmaceuticals

Identifier:

  • LOC-100007939

Status: Valid (2008-10-31)

Package 1 of 1

PCID:

Description:
Blister, 100 tablet

Marketing status:

  • Kingdom of Sweden: Marketed

Pack size:

  • 100 Tablet

Package: 1 Box (Cardboard)

Containing:

Package: 10 Blister (Aluminium)

Containing: 10 Tablet

Manufactured Item

Dose form: Film-coated tablet

Unit of presentation: Tablet

Ingredient

Role: Active

Substance: Simvastatin

Presentation strength: 20 milligram(s) / 1 tablet

Reference strength:
Simvastatin 20 milligram(s) / 1 tablet

Administrable Product (1 of 1)

Dose form: Film-coated tablet

Unit of presentation:

Route of administration:

  • Oral use

Ingredients:

Ingredient

Role: Active

Substance: Simvastatin

Presentation strength: 20 milligram(s) / 1 tablet

Reference strength:
Simvastatin 20 milligram(s) / 1 tablet