Valsartan Zentiva 80 mg

Valsartan Zentiva 80 mg is a medicine authorised by Swissmedic under authorisation number 61491. 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 03 August 2011 and the authorisation is valid without a time limit. ATC code C09CA03 places the medicine in the group Agents acting on the renin-angiotensin system.

  • Dispensing category B
  • Authorisation number 61491
  • ATC C09CA03
  • Synthetic medicines
Authorisation data
Authorisation number61491
NameValsartan Zentiva 80 mg
Full nameValsartan Zentiva 80 mg, Filmtabletten
Authorisation holderHelvepharm AG
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeC09CA03
First authorisation03 August 2011
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Valsartan Zentiva 80 mg, FilmtablettenB03 August 2011
3Valsartan Zentiva 40 mg, FilmtablettenB03 August 2011
4Valsartan Zentiva 160 mg, FilmtablettenB08 August 2012

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
828Tablette(n)C09CA0302.07.1.B
998Tablette(n)C09CA0302.07.1.B
1028Tablette(n)C09CA0302.07.1.B
1128Tablette(n)C09CA0302.07.1.B
1298Tablette(n)C09CA0302.07.1.B

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Valsartan Zentiva 80 mg authorised in Switzerland?

Yes. Valsartan Zentiva 80 mg is authorised by Swissmedic under authorisation number 61491, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Valsartan Zentiva 80 mg have?

Valsartan Zentiva 80 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 Valsartan Zentiva 80 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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