VeraSeal 2 ml
VeraSeal 2 ml is a medicine authorised by Swissmedic under authorisation number 67975. The authorisation holder is Janssen-Cilag AG. 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 May 2021 and the authorisation is valid without a time limit. ATC code B02BC places the medicine in the group Antihemorrhagics.
| Authorisation number | 67975 |
|---|---|
| Name | VeraSeal 2 ml |
| Full name | VeraSeal 2 ml, Lösung für Gewebekleber |
| Authorisation holder | Janssen-Cilag AG |
| Medicinal product code | Blood products |
| Dispensing category | B · Prescription only |
| ATC code | B02BC |
| First authorisation | 20 May 2021 |
| Authorisation validity | unlimited |
| No. | Name | Dispensing category | Authorisation date |
|---|---|---|---|
| 1 | VeraSeal 2 ml, Lösung für Gewebekleber | B | 20 May 2021 |
| 2 | VeraSeal 4 ml, Lösung für Gewebekleber | B | 20 May 2021 |
| 3 | VeraSeal 6 ml, Lösung für Gewebekleber | B | 20 May 2021 |
| 4 | VeraSeal 10 ml, Lösung für Gewebekleber | B | 20 May 2021 |
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| Pack code | Quantity | Unit | ATC | IT code | Dispensing category |
|---|---|---|---|---|---|
| 1 | 2x 1 ml | Fertigspritze(n) | B02BC | 06.99.0. | B |
| 2 | 2x 2 ml | Fertigspritze(n) | B02BC | 06.99.0. | B |
| 3 | 2x 3 ml | Fertigspritze(n) | B02BC | 06.99.0. | B |
| 4 | 2x 5 ml | Fertigspritze(n) | B02BC | 06.99.0. | B |
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Other medicines from this authorisation holder
Frequently asked questions
Is VeraSeal 2 ml authorised in Switzerland?
Yes. VeraSeal 2 ml is authorised by Swissmedic under authorisation number 67975, data as of 01 September 2026. The authorisation is valid without a time limit.
Which dispensing category does VeraSeal 2 ml have?
VeraSeal 2 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 VeraSeal 2 ml?
The authorisation holder is Janssen-Cilag 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.