Pitavastatin Zentiva 1 mg

Pitavastatin Zentiva 1 mg is a medicine authorised by Swissmedic under authorisation number 68219. 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 18 July 2022 and the authorisation is limited until 17 July 2027. ATC code C10AA08 places the medicine in the group Lipid modifying agents.

  • Dispensing category B
  • Authorisation number 68219
  • ATC C10AA08
  • Synthetic medicines
Authorisation data
Authorisation number68219
NamePitavastatin Zentiva 1 mg
Full namePitavastatin Zentiva 1 mg, Filmtabletten
Authorisation holderHelvepharm AG
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeC10AA08
First authorisation18 July 2022
Authorisation validity17 July 2027
Strengths
No.NameDispensing categoryAuthorisation date
1Pitavastatin Zentiva 1 mg, FilmtablettenB18 July 2022
2Pitavastatin Zentiva 2 mg, FilmtablettenB18 July 2022
3Pitavastatin Zentiva 4 mg, FilmtablettenB18 July 2022

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
128Tablette(n)C10AA0807.12.0.B
284Tablette(n)C10AA0807.12.0.B
328Tablette(n)C10AA0807.12.0.B
484Tablette(n)C10AA0807.12.0.B
528Tablette(n)C10AA0807.12.0.B
684Tablette(n)C10AA0807.12.0.B

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Pitavastatin Zentiva 1 mg authorised in Switzerland?

Yes. Pitavastatin Zentiva 1 mg is authorised by Swissmedic under authorisation number 68219, data as of 01 September 2026. The authorisation is limited until 17 July 2027.

Which dispensing category does Pitavastatin Zentiva 1 mg have?

Pitavastatin Zentiva 1 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 Pitavastatin Zentiva 1 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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