Micardis Amlo 40/5 mg

Micardis Amlo 40/5 mg is a medicine authorised by Swissmedic under authorisation number 61270. The authorisation holder is Boehringer Ingelheim (Schweiz) GmbH. 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 08 November 2010 and the authorisation is valid without a time limit. ATC code C09DB04 places the medicine in the group Agents acting on the renin-angiotensin system.

  • Dispensing category B
  • Authorisation number 61270
  • ATC C09DB04
  • Synthetic medicines
Authorisation data
Authorisation number61270
NameMicardis Amlo 40/5 mg
Full nameMicardis Amlo 40/5 mg, Tabletten
Authorisation holderBoehringer Ingelheim (Schweiz) GmbH
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeC09DB04
First authorisation08 November 2010
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Micardis Amlo 40/5 mg, TablettenB08 November 2010
3Micardis Amlo 80/5 mg, TablettenB08 November 2010
4Micardis Amlo 80/10 mg, TablettenB08 November 2010

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
128Tablette(n)C09DB0402.07.2.B
298Tablette(n)C09DB0402.07.2.B
528Tablette(n)C09DB0402.07.2.B
698Tablette(n)C09DB0402.07.2.B
728Tablette(n)C09DB0402.07.2.B
898Tablette(n)C09DB0402.07.2.B

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Other medicines from this authorisation holder

Frequently asked questions

Is Micardis Amlo 40/5 mg authorised in Switzerland?

Yes. Micardis Amlo 40/5 mg is authorised by Swissmedic under authorisation number 61270, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Micardis Amlo 40/5 mg have?

Micardis Amlo 40/5 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 Micardis Amlo 40/5 mg?

The authorisation holder is Boehringer Ingelheim (Schweiz) GmbH. 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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