Entresto 50 mg

Entresto 50 mg is a medicine authorised by Swissmedic under authorisation number 65673. The authorisation holder is Novartis Pharma Schweiz 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 17 September 2015 and the authorisation is valid without a time limit. ATC code C09DX04 places the medicine in the group Agents acting on the renin-angiotensin system.

  • Dispensing category B
  • Authorisation number 65673
  • ATC C09DX04
  • Synthetic medicines
Authorisation data
Authorisation number65673
NameEntresto 50 mg
Full nameEntresto 50 mg, Filmtabletten
Authorisation holderNovartis Pharma Schweiz AG
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeC09DX04
First authorisation17 September 2015
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Entresto 50 mg, FilmtablettenB17 September 2015
2Entresto 100 mg, FilmtablettenB17 September 2015
3Entresto 200 mg, FilmtablettenB17 September 2015

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
128Tablette(n)C09DX0402.07.2.B
656Tablette(n)C09DX0402.07.2.B
256Tablette(n)C09DX0402.07.2.B
7168Tablette(n)C09DX0402.07.2.B
456Tablette(n)C09DX0402.07.2.B
8168Tablette(n)C09DX0402.07.2.B

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Entresto 50 mg authorised in Switzerland?

Yes. Entresto 50 mg is authorised by Swissmedic under authorisation number 65673, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Entresto 50 mg have?

Entresto 50 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 Entresto 50 mg?

The authorisation holder is Novartis Pharma Schweiz 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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