UnicomIG
0.1.0 - ci-build

UnicomIG, 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/hl7-eu/unicom-ig/tree/master and changes regularly. See the Directory of published versions

Example Bundle: 006-Yaz-002mg3mg-tablet-SE-FullProduct

Yaz 0,02 mg/3 mg Filmdragerad tablett

MPID: SE-100004813-00026267

Full name: Yaz 0,02 mg/3 mg Filmdragerad tablett

- Invented name part: Yaz

- Strength part: 0,02 mg/3 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:

  • 100000095785 drospirenone and ethinylestradiol

Marketing Authorisation 1 of 1

Authorisation number: 26267

Region: Kingdom of Sweden

Marketing authorisation holder: Bayer AB

Identifier:

  • LOC-100016468

Status: Valid (2008-07-03)

Package 1 of 1

PCID:

Description:
Blister, 3 x 28 tabletter

Marketing status:

  • Kingdom of Sweden: Marketed

Pack size:

  • 84 tablet

Package: 1 Box (Plastic)

Containing:

Package: 3 Box (Cardboard)

Containing:

Package: 1 Blister (Aluminium) (PolyVinyl Chloride)

Containing: 24 tablet

Manufactured Item

Dose form: Film-coated tablet

Unit of presentation: tablet

Ingredient

Role: Active

Substance: Ethinylestradiol betadex clathrate

Presentation strength: 173.17 microgram(s) / 1 tablet

Reference strength:
Ethinylestradiol 20 microgram(s) / 1 tablet

Ingredient

Role: Active

Substance: drospirenone

Presentation strength: 3 milligram(s) / 1 tablet

Reference strength:
drospirenone 3 milligram(s) / 1 tablet

4 tablet

Manufactured Item

Dose form: Film-coated tablet

Unit of presentation: tablet

Ingredient

Role: Excipient

Substance: Lactose monohydrate

Presentation strength: 23.2 milligram(s) / 1 tablet

Reference strength:
lactose 22 milligram(s) / 1 tablet

Administrable Product (1 of 2)

Dose form: Film-coated tablet

Unit of presentation:

Route of administration:

  • Oral use

Ingredients:

Ingredient

Role: Active

Substance: Ethinylestradiol betadex clathrate

Presentation strength: 173.17 microgram(s) / 1 tablet

Reference strength:
Ethinylestradiol 20 microgram(s) / 1 tablet

Ingredient

Role: Active

Substance: drospirenone

Presentation strength: 3 milligram(s) / 1 tablet

Reference strength:
drospirenone 3 milligram(s) / 1 tablet

Administrable Product (2 of 2)

Dose form: Film-coated tablet

Unit of presentation:

Route of administration:

  • Oral use

Ingredients:

Ingredient

Role: Excipient

Substance: Lactose monohydrate

Presentation strength: 23.2 milligram(s) / 1 tablet

Reference strength:
lactose 22 milligram(s) / 1 tablet