Etoricoxib Zentiva 30 mg
Etoricoxib Zentiva 30 mg is a medicine authorised by Swissmedic under authorisation number 68245. The authorisation holder is Helvepharm 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 24 February 2022 and the authorisation is limited until 23 February 2027. ATC code M01AH05 places the medicine in the group Anti-inflammatory and antirheumatic products.
| Authorisation number | 68245 |
|---|---|
| Name | Etoricoxib Zentiva 30 mg |
| Full name | Etoricoxib Zentiva 30 mg, Filmtabletten |
| Authorisation holder | Helvepharm AG |
| Medicinal product code | Synthetic medicines |
| Dispensing category | B · Prescription only |
| ATC code | M01AH05 |
| First authorisation | 24 February 2022 |
| Authorisation validity | 23 February 2027 |
| No. | Name | Dispensing category | Authorisation date |
|---|---|---|---|
| 1 | Etoricoxib Zentiva 30 mg, Filmtabletten | B | 24 February 2022 |
| 2 | Etoricoxib Zentiva 60 mg, Filmtabletten | B | 24 February 2022 |
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| Pack code | Quantity | Unit | ATC | IT code | Dispensing category |
|---|---|---|---|---|---|
| 1 | 28 | Tablette(n) | M01AH05 | 07.10.1. | B |
| 2 | 7 | Tablette(n) | M01AH05 | 07.10.1. | B |
| 3 | 28 | Tablette(n) | M01AH05 | 07.10.1. | B |
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Medicines in the same ATC group
Other medicines from this authorisation holder
Frequently asked questions
Is Etoricoxib Zentiva 30 mg authorised in Switzerland?
Yes. Etoricoxib Zentiva 30 mg is authorised by Swissmedic under authorisation number 68245, data as of 01 September 2026. The authorisation is limited until 23 February 2027.
Which dispensing category does Etoricoxib Zentiva 30 mg have?
Etoricoxib Zentiva 30 mg 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 Etoricoxib Zentiva 30 mg?
The authorisation holder is Helvepharm 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.