Naproxen Esomeprazol Sandoz 500 mg / 20 mg

Naproxen Esomeprazol Sandoz 500 mg / 20 mg is a medicine authorised by Swissmedic under authorisation number 69184. The authorisation holder is Sandoz Pharmaceuticals 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 19 November 2024 and the authorisation is limited until 18 November 2029. ATC code M01AE52 places the medicine in the group Anti-inflammatory and antirheumatic products.

  • Dispensing category B
  • Authorisation number 69184
  • ATC M01AE52
  • Synthetic medicines
Authorisation data
Authorisation number69184
NameNaproxen Esomeprazol Sandoz 500 mg / 20 mg
Full nameNaproxen Esomeprazol Sandoz 500 mg / 20 mg, Filmtabletten
Authorisation holderSandoz Pharmaceuticals AG
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeM01AE52
First authorisation19 November 2024
Authorisation validity18 November 2029
Strengths
No.NameDispensing categoryAuthorisation date
1Naproxen Esomeprazol Sandoz 500 mg / 20 mg, FilmtablettenB19 November 2024

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
130Tablette(n)M01AE5207.10.2.B
260Tablette(n)M01AE5207.10.2.B

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Naproxen Esomeprazol Sandoz 500 mg / 20 mg authorised in Switzerland?

Yes. Naproxen Esomeprazol Sandoz 500 mg / 20 mg is authorised by Swissmedic under authorisation number 69184, data as of 01 September 2026. The authorisation is limited until 18 November 2029.

Which dispensing category does Naproxen Esomeprazol Sandoz 500 mg / 20 mg have?

Naproxen Esomeprazol Sandoz 500 mg / 20 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 Naproxen Esomeprazol Sandoz 500 mg / 20 mg?

The authorisation holder is Sandoz Pharmaceuticals 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.

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