Eprex 1000 U
Eprex 1000 U is a medicine authorised by Swissmedic under authorisation number 49078. The authorisation holder is Janssen-Cilag AG. The medicinal product code is Biotechnological 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 27 July 1988 and the authorisation is valid without a time limit. ATC code B03XA01 places the medicine in the group Antianemic preparations.
| Authorisation number | 49078 |
|---|---|
| Name | Eprex 1000 U |
| Full name | Eprex 1000 U, Injektionslösung (Fertigspritzen) |
| Authorisation holder | Janssen-Cilag AG |
| Medicinal product code | Biotechnological medicines |
| Dispensing category | A · Prescription, not repeatable |
| ATC code | B03XA01 |
| First authorisation | 27 July 1988 |
| Authorisation validity | unlimited |
| No. | Name | Dispensing category | Authorisation date |
|---|---|---|---|
| 18 | Eprex 1000 U, Injektionslösung (Fertigspritzen) | A | 24 July 1998 |
| 19 | Eprex 2000 U, Injektionslösung (Fertigspritzen) | A | 27 July 1998 |
| 20 | Eprex 3000 U, Injektionslösung (Fertigspritzen) | A | 24 July 1998 |
| 21 | Eprex 4000 U, Injektionslösung (Fertigspritzen) | A | 24 July 1998 |
| 22 | Eprex 10000 U, Injektionslösung (Fertigspritzen) | A | 24 July 1998 |
| 36 | Eprex 20000 U, Injektionslösung (Fertigspritzen) | A | 07 December 2000 |
| 37 | Eprex 40000 U, Injektionslösung (Fertigspritzen) | A | 07 December 2000 |
| 38 | Eprex 5000 U, Injektionslösung (Fertigspritzen) | A | 07 December 2000 |
| 39 | Eprex 6000 U, Injektionslösung (Fertigspritzen) | A | 07 December 2000 |
| 41 | Eprex 8000 U, Injektionslösung (Fertigspritzen) | A | 07 December 2000 |
| 43 | Eprex 30000 U, Injektionslösung (Fertigspritzen) | A | 06 June 2007 |
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| Pack code | Quantity | Unit | ATC | IT code | Dispensing category |
|---|---|---|---|---|---|
| 804 | 6 x 0,5 mL | Spritze(n) | B03XA01 | 06.07.3. | A |
| 805 | 6 x 0,5 mL | Spritze(n) | B03XA01 | 06.07.3. | A |
| 806 | 6 x 0,3 mL | Spritze(n) | B03XA01 | 06.07.3. | A |
| 807 | 6 x 0,4 mL | Spritze(n) | B03XA01 | 06.07.3. | A |
| 808 | 6 x 1 mL | Spritze(n) | B03XA01 | 06.07.3. | A |
| 809 | 1 x 0,5 mL | Spritze(n) | B03XA01 | 06.07.3. | A |
| 810 | 4 x 1 mL | Spritze(n) | B03XA01 | 06.07.3. | A |
| 811 | 1 x 1 mL | Spritze(n) | B03XA01 | 06.07.3. | A |
| 812 | 6 x 0.5 mL | Spritze(n) | B03XA01 | 06.07.3. | A |
| 813 | 6 x 0,6 mL | Spritze(n) | B03XA01 | 06.07.3. | A |
| 814 | 6 x 0,8 mL | Spritze(n) | B03XA01 | 06.07.3. | A |
| 815 | 1 x 0,75 mL | Spritze(n) | B03XA01 | 06.07.3. | A |
| 816 | 4 x 0,75 mL | Spritze(n) | B03XA01 | 06.07.3. | A |
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Medicines in the same ATC group
Other medicines from this authorisation holder
Frequently asked questions
Is Eprex 1000 U authorised in Switzerland?
Yes. Eprex 1000 U is authorised by Swissmedic under authorisation number 49078, data as of 01 September 2026. The authorisation is valid without a time limit.
Which dispensing category does Eprex 1000 U have?
Eprex 1000 U 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 Eprex 1000 U?
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.