Metformin Zentiva 500 mg

Metformin Zentiva 500 mg is a medicine authorised by Swissmedic under authorisation number 68223. 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 16 May 2022 and the authorisation is limited until 15 May 2027. ATC code A10BA02 places the medicine in the group Drugs used in diabetes.

  • Dispensing category B
  • Authorisation number 68223
  • ATC A10BA02
  • Synthetic medicines
Authorisation data
Authorisation number68223
NameMetformin Zentiva 500 mg
Full nameMetformin Zentiva 500 mg, Filmtabletten
Authorisation holderHelvepharm AG
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeA10BA02
First authorisation16 May 2022
Authorisation validity15 May 2027
Strengths
No.NameDispensing categoryAuthorisation date
1Metformin Zentiva 500 mg, FilmtablettenB16 May 2022
2Metformin Zentiva 850 mg, FilmtablettenB16 May 2022
3Metformin Zentiva 1000 mg, FilmtablettenB16 May 2022

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
1360Tablette(n)A10BA0207.06.2.B
1440Tablette(n)A10BA0207.06.2.B
15100Tablette(n)A10BA0207.06.2.B
1660Tablette(n)A10BA0207.06.2.B
17120Tablette(n)A10BA0207.06.2.B

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Metformin Zentiva 500 mg authorised in Switzerland?

Yes. Metformin Zentiva 500 mg is authorised by Swissmedic under authorisation number 68223, data as of 01 September 2026. The authorisation is limited until 15 May 2027.

Which dispensing category does Metformin Zentiva 500 mg have?

Metformin Zentiva 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 Metformin Zentiva 500 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.

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