Renvela

Renvela is a medicine authorised by Swissmedic under authorisation number 61648. The authorisation holder is Sanofi-Aventis (Suisse) SA. 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 10 November 2011 and the authorisation is valid without a time limit. ATC code V03AE02 places the medicine in the group All other therapeutic products.

  • Dispensing category B
  • Authorisation number 61648
  • ATC V03AE02
  • Synthetic medicines
Authorisation data
Authorisation number61648
NameRenvela
Full nameRenvela, comprimés pelliculés
Authorisation holderSanofi-Aventis (Suisse) SA
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeV03AE02
First authorisation10 November 2011
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Renvela, comprimés pelliculésB10 November 2011

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
1180Tablette(n)V03AE0207.99.0.B

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Renvela authorised in Switzerland?

Yes. Renvela is authorised by Swissmedic under authorisation number 61648, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Renvela have?

Renvela 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 Renvela?

The authorisation holder is Sanofi-Aventis (Suisse) SA. 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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