LatanoTim-Vision SDU 50 µg / ml + 5 mg / ml

LatanoTim-Vision SDU 50 µg / ml + 5 mg / ml is a medicine authorised by Swissmedic under authorisation number 70651. The authorisation holder is OmniVision 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 26 May 2026 and the authorisation is limited until 25 May 2031. ATC code S01ED51 places the medicine in the group Ophthalmologicals.

  • Dispensing category B
  • Authorisation number 70651
  • ATC S01ED51
  • Synthetic medicines
Authorisation data
Authorisation number70651
NameLatanoTim-Vision SDU 50 µg / ml + 5 mg / ml
Full nameLatanoTim-Vision SDU 50 µg / ml + 5 mg / ml, Augentropfen, Lösung im Einzeldosisbehältnis
Authorisation holderOmniVision AG
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeS01ED51
First authorisation26 May 2026
Authorisation validity25 May 2031
Strengths
No.NameDispensing categoryAuthorisation date
1LatanoTim-Vision SDU 50 µg / ml + 5 mg / ml, Augentropfen, Lösung im EinzeldosisbehältnisB26 May 2026

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
130Einzeldose(n)S01ED5111.09.0.B
290Einzeldose(n)S01ED5111.09.0.B

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is LatanoTim-Vision SDU 50 µg / ml + 5 mg / ml authorised in Switzerland?

Yes. LatanoTim-Vision SDU 50 µg / ml + 5 mg / ml is authorised by Swissmedic under authorisation number 70651, data as of 01 September 2026. The authorisation is limited until 25 May 2031.

Which dispensing category does LatanoTim-Vision SDU 50 µg / ml + 5 mg / ml have?

LatanoTim-Vision SDU 50 µg / ml + 5 mg / ml 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 LatanoTim-Vision SDU 50 µg / ml + 5 mg / ml?

The authorisation holder is OmniVision 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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