Uman Albumin Kedrion 200 g/I
Uman Albumin Kedrion 200 g/I is a medicine authorised by Swissmedic under authorisation number 58155. The authorisation holder is Dudler Pharma Sàrl. The medicinal product code is Blood products and the dispensing category is B: Supplied only against a prescription which, at the prescriber's discretion, may be dispensed repeatedly. First authorisation was granted on 20 February 2008 and the authorisation is valid without a time limit. ATC code B05AA01 places the medicine in the group Blood substitutes and perfusion solutions.
| Authorisation number | 58155 |
|---|---|
| Name | Uman Albumin Kedrion 200 g/I |
| Full name | Uman Albumin Kedrion 200 g/I, solution pour perfusion |
| Authorisation holder | Dudler Pharma Sàrl |
| Medicinal product code | Blood products |
| Dispensing category | B · Prescription only |
| ATC code | B05AA01 |
| First authorisation | 20 February 2008 |
| Authorisation validity | unlimited |
| No. | Name | Dispensing category | Authorisation date |
|---|---|---|---|
| 1 | Uman Albumin Kedrion 200 g/I, solution pour perfusion | B | 20 February 2008 |
| 2 | Uman Albumin Kedrion 250 g/l, solution pour perfusion | B | 20 February 2008 |
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| Pack code | Quantity | Unit | ATC | IT code | Dispensing category |
|---|---|---|---|---|---|
| 1 | 50 | ml | B05AA01 | 06.01.1. | B |
| 2 | 100 | ml | B05AA01 | 06.01.1. | B |
| 3 | 50 | ml | B05AA01 | 06.01.1. | B |
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Medicines in the same ATC group
Other medicines from this authorisation holder
Frequently asked questions
Is Uman Albumin Kedrion 200 g/I authorised in Switzerland?
Yes. Uman Albumin Kedrion 200 g/I is authorised by Swissmedic under authorisation number 58155, data as of 01 September 2026. The authorisation is valid without a time limit.
Which dispensing category does Uman Albumin Kedrion 200 g/I have?
Uman Albumin Kedrion 200 g/I is in dispensing category B. Supplied only against a prescription which, at the prescriber's discretion, may be dispensed repeatedly.
Who is the authorisation holder of Uman Albumin Kedrion 200 g/I?
The authorisation holder is Dudler Pharma Sàrl. The holder carries the legal responsibility for quality, safety and product information of the medicine in Switzerland.
Sources
Swissmedic data as of 01 September 2026. No medical advice. Independent directory, not affiliated with Swissmedic or the FOPH.