Xiidra

Xiidra is a medicine authorised by Swissmedic under authorisation number 66850. The authorisation holder is Bausch & Lomb Swiss 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 19 December 2018 and the authorisation is valid without a time limit. ATC code S01XA25 places the medicine in the group Ophthalmologicals.

  • Dispensing category B
  • Authorisation number 66850
  • ATC S01XA25
  • Synthetic medicines
Authorisation data
Authorisation number66850
NameXiidra
Full nameXiidra, Augentropfen
Authorisation holderBausch & Lomb Swiss AG
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeS01XA25
First authorisation19 December 2018
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Xiidra, AugentropfenB19 December 2018

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
260 x 0.2mlS01XA2511.99.0.B

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Other medicines from this authorisation holder

Frequently asked questions

Is Xiidra authorised in Switzerland?

Yes. Xiidra is authorised by Swissmedic under authorisation number 66850, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Xiidra have?

Xiidra 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 Xiidra?

The authorisation holder is Bausch & Lomb Swiss 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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