Ramipril HCT Zentiva 2.5/12.5 mg

Ramipril HCT Zentiva 2.5/12.5 mg is a medicine authorised by Swissmedic under authorisation number 58177. 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 07 May 2007 and the authorisation is valid without a time limit. ATC code C09BA05 places the medicine in the group Agents acting on the renin-angiotensin system.

  • Dispensing category B
  • Authorisation number 58177
  • ATC C09BA05
  • Synthetic medicines
Authorisation data
Authorisation number58177
NameRamipril HCT Zentiva 2.5/12.5 mg
Full nameRamipril HCT Zentiva 2.5/12.5 mg, Tabletten
Authorisation holderHelvepharm AG
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeC09BA05
First authorisation07 May 2007
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Ramipril HCT Zentiva 2.5/12.5 mg, TablettenB07 May 2007
2Ramipril HCT Zentiva 5/25 mg, TablettenB07 May 2007

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
920Tablette(n)C09BA0502.07.2.B
10100Tablette(n)C09BA0502.07.2.B
1120Tablette(n)C09BA0502.07.2.B
12100Tablette(n)C09BA0502.07.2.B

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Ramipril HCT Zentiva 2.5/12.5 mg authorised in Switzerland?

Yes. Ramipril HCT Zentiva 2.5/12.5 mg is authorised by Swissmedic under authorisation number 58177, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Ramipril HCT Zentiva 2.5/12.5 mg have?

Ramipril HCT Zentiva 2.5/12.5 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 Ramipril HCT Zentiva 2.5/12.5 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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