Janumet XR 50 mg/500 mg

Janumet XR 50 mg/500 mg is a medicine authorised by Swissmedic under authorisation number 65052. The authorisation holder is MSD Merck Sharp & Dohme 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 30 July 2014 and the authorisation is valid without a time limit. ATC code A10BD07 places the medicine in the group Drugs used in diabetes.

  • Dispensing category B
  • Authorisation number 65052
  • ATC A10BD07
  • Synthetic medicines
Authorisation data
Authorisation number65052
NameJanumet XR 50 mg/500 mg
Full nameJanumet XR 50 mg/500 mg, Filmtabletten
Authorisation holderMSD Merck Sharp & Dohme AG
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeA10BD07
First authorisation30 July 2014
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Janumet XR 50 mg/500 mg, FilmtablettenB30 July 2014
2Janumet XR 50 mg/1000 mg, FilmtablettenB30 July 2014
3Janumet XR 100 mg/1000 mg, FilmtablettenB30 July 2014

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
256Tablette(n)A10BD0707.06.2.B
7168Tablette(n)A10BD0707.06.2.B
456Tablette(n)A10BD0707.06.2.B
8168Tablette(n)A10BD0707.06.2.B
528Tablette(n)A10BD0707.06.2.B
984Tablette(n)A10BD0707.06.2.B

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Janumet XR 50 mg/500 mg authorised in Switzerland?

Yes. Janumet XR 50 mg/500 mg is authorised by Swissmedic under authorisation number 65052, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Janumet XR 50 mg/500 mg have?

Janumet XR 50 mg/500 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 Janumet XR 50 mg/500 mg?

The authorisation holder is MSD Merck Sharp & Dohme 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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