Nordimet 7.5 mg/0.3 ml
Nordimet 7.5 mg/0.3 ml is a medicine authorised by Swissmedic under authorisation number 65839. The authorisation holder is Nordic Pharma GmbH. The medicinal product code is Synthetic medicines and the dispensing category is A: Supplied only against a medical or veterinary prescription that may not be dispensed repeatedly. First authorisation was granted on 21 October 2016 and the authorisation is valid without a time limit. ATC code L04AX03 places the medicine in the group Immunosuppressants.
| Authorisation number | 65839 |
|---|---|
| Name | Nordimet 7.5 mg/0.3 ml |
| Full name | Nordimet 7.5 mg/0.3 ml, Injektionslösung in einer Fertigspritze |
| Authorisation holder | Nordic Pharma GmbH |
| Medicinal product code | Synthetic medicines |
| Dispensing category | A · Prescription, not repeatable |
| ATC code | L04AX03 |
| First authorisation | 21 October 2016 |
| Authorisation validity | unlimited |
| No. | Name | Dispensing category | Authorisation date |
|---|---|---|---|
| 1 | Nordimet 7.5 mg/0.3 ml, Injektionslösung in einer Fertigspritze | A | 21 October 2016 |
| 2 | Nordimet 10.0 mg/0.4 ml, Injektionslösung in einer Fertigspritze | A | 21 October 2016 |
| 3 | Nordimet 12.5 mg/0.5 ml, Injektionslösung in einer Fertigspritze | A | 21 October 2016 |
| 4 | Nordimet 15.0 mg/0.6 ml, Injektionslösung in einer Fertigspritze | A | 21 October 2016 |
| 5 | Nordimet 17.5 mg/0.7 ml, Injektionslösung in einer Fertigspritze | A | 21 October 2016 |
| 6 | Nordimet 20.0 mg/0.8 ml, Injektionslösung in einer Fertigspritze | A | 21 October 2016 |
| 7 | Nordimet 22.5 mg/0.9 ml, Injektionslösung in einer Fertigspritze | A | 21 October 2016 |
| 8 | Nordimet 25 mg/1.0 ml, Injektionslösung in einer Fertigspritze | A | 21 October 2016 |
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| Pack code | Quantity | Unit | ATC | IT code | Dispensing category |
|---|---|---|---|---|---|
| 1 | 1 | Fertigspritze(n) | L04AX03 | 07.10.6. | A |
| 2 | 4 | Fertigspritze(n) | L04AX03 | 07.10.6. | A |
| 4 | 1 | Fertigspritze(n) | L04AX03 | 07.10.6. | A |
| 5 | 4 | Fertigspritze(n) | L04AX03 | 07.10.6. | A |
| 7 | 1 | Fertigspritze(n) | L04AX03 | 07.10.6. | A |
| 8 | 4 | Fertigspritze(n) | L04AX03 | 07.10.6. | A |
| 10 | 1 | Fertigspritze(n) | L04AX03 | 07.10.6. | A |
| 11 | 4 | Fertigspritze(n) | L04AX03 | 07.10.6. | A |
| 13 | 1 | Fertigspritze(n) | L04AX03 | 07.10.6. | A |
| 14 | 4 | Fertigspritze(n) | L04AX03 | 07.10.6. | A |
| 16 | 1 | Fertigspritze(n) | L04AX03 | 07.10.6. | A |
| 17 | 4 | Fertigspritze(n) | L04AX03 | 07.10.6. | A |
| 19 | 1 | Fertigspritze(n) | L04AX03 | 07.10.6. | A |
| 20 | 4 | Fertigspritze(n) | L04AX03 | 07.10.6. | A |
| 22 | 1 | Fertigspritze(n) | L04AX03 | 07.10.6. | A |
| 23 | 4 | Fertigspritze(n) | L04AX03 | 07.10.6. | A |
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Medicines in the same ATC group
Other medicines from this authorisation holder
Frequently asked questions
Is Nordimet 7.5 mg/0.3 ml authorised in Switzerland?
Yes. Nordimet 7.5 mg/0.3 ml is authorised by Swissmedic under authorisation number 65839, data as of 01 September 2026. The authorisation is valid without a time limit.
Which dispensing category does Nordimet 7.5 mg/0.3 ml have?
Nordimet 7.5 mg/0.3 ml is in dispensing category A. Supplied only against a medical or veterinary prescription that may not be dispensed repeatedly.
Who is the authorisation holder of Nordimet 7.5 mg/0.3 ml?
The authorisation holder is Nordic Pharma GmbH. 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.