Losartan Zentiva 12.5 mg

Losartan Zentiva 12.5 mg is a medicine authorised by Swissmedic under authorisation number 60234. 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 14 January 2011 and the authorisation is valid without a time limit. ATC code C09CA01 places the medicine in the group Agents acting on the renin-angiotensin system.

  • Dispensing category B
  • Authorisation number 60234
  • ATC C09CA01
  • Synthetic medicines
Authorisation data
Authorisation number60234
NameLosartan Zentiva 12.5 mg
Full nameLosartan Zentiva 12.5 mg, Filmtabletten
Authorisation holderHelvepharm AG
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeC09CA01
First authorisation14 January 2011
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Losartan Zentiva 12.5 mg, FilmtablettenB14 January 2011
3Losartan Zentiva 50 mg, FilmtablettenB14 January 2011
4Losartan Zentiva 100 mg, FilmtablettenB14 January 2011

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
1310Tablette(n)C09CA0102.07.1.B
1428Tablette(n)C09CA0102.07.1.B
1598Tablette(n)C09CA0102.07.1.B
1628Tablette(n)C09CA0102.07.1.B
1798Tablette(n)C09CA0102.07.1.B

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Losartan Zentiva 12.5 mg authorised in Switzerland?

Yes. Losartan Zentiva 12.5 mg is authorised by Swissmedic under authorisation number 60234, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Losartan Zentiva 12.5 mg have?

Losartan Zentiva 12.5 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 Losartan Zentiva 12.5 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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