Remodulin 1 mg/ml
Remodulin 1 mg/ml is a medicine authorised by Swissmedic under authorisation number 56120. The authorisation holder is Gebro Pharma AG. The medicinal product code is Synthetic medicines 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 26 November 2004 and the authorisation is valid without a time limit. ATC code B01AC21 places the medicine in the group Antithrombotic agents.
| Authorisation number | 56120 |
|---|---|
| Name | Remodulin 1 mg/ml |
| Full name | Remodulin 1 mg/ml, Infusionslösung s.c. und i.v. |
| Authorisation holder | Gebro Pharma AG |
| Medicinal product code | Synthetic medicines |
| Dispensing category | B · Prescription only |
| ATC code | B01AC21 |
| First authorisation | 26 November 2004 |
| Authorisation validity | unlimited |
| No. | Name | Dispensing category | Authorisation date |
|---|---|---|---|
| 1 | Remodulin 1 mg/ml, Infusionslösung s.c. und i.v. | B | 26 November 2004 |
| 2 | Remodulin 2.5 mg/ml, Infusionslösung s.c. und i.v. | B | 26 November 2004 |
| 5 | Remodulin 5 mg/ml, Infusionslösung s.c und i.v. | B | 16 May 2012 |
| 6 | Remodulin 10 mg/ml, Infusionslösung s.c. und i.v. | B | 16 May 2012 |
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| Pack code | Quantity | Unit | ATC | IT code | Dispensing category |
|---|---|---|---|---|---|
| 1 | 1 x 20 ml | Durchstechflasche(n) | B01AC21 | 02.07.1. | B |
| 3 | 1 x 20 ml | Durchstechflasche(n) | B01AC21 | 02.07.1. | B |
| 4 | 1 x 20 ml | Durchstechflasche(n) | B01AC21 | 02.07.1. | B |
| 5 | 1 x 20 ml | Durchstechflasche(n) | B01AC21 | 02.07.1. | B |
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Medicines in the same ATC group
Other medicines from this authorisation holder
Frequently asked questions
Is Remodulin 1 mg/ml authorised in Switzerland?
Yes. Remodulin 1 mg/ml is authorised by Swissmedic under authorisation number 56120, data as of 01 September 2026. The authorisation is valid without a time limit.
Which dispensing category does Remodulin 1 mg/ml have?
Remodulin 1 mg/ml 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 Remodulin 1 mg/ml?
The authorisation holder is Gebro Pharma AG. 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.