Yaldigo 400 mg

Yaldigo 400 mg is a medicine authorised by Swissmedic under authorisation number 53108. The authorisation holder is Tillotts Pharma 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 15 November 1994 and the authorisation is valid without a time limit. ATC code A07EC02 places the medicine in the group Antidiarrheals, intestinal anti-inflammatory and anti-infective agents.

  • Dispensing category B
  • Authorisation number 53108
  • ATC A07EC02
  • Synthetic medicines
Authorisation data
Authorisation number53108
NameYaldigo 400 mg
Full nameYaldigo 400 mg, magensaftresistente Tablette
Authorisation holderTillotts Pharma AG
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeA07EC02
First authorisation15 November 1994
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Yaldigo 400 mg, magensaftresistente TabletteB15 November 1994
2Yaldigo 800 mg, magensaftesistente TabletteB25 September 2002
3Yaldigo 1600 mg, magensaftresistente TabletteB17 July 2019

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
4100Tablette(n)A07EC0204.09.0.B
590Tablette(n)A07EC0204.09.0.B
730Tablette(n)A07EC0204.09.0.B
130Tablette(n)A07EC0204.09.0.B
260Tablette(n)A07EC0204.09.0.B
390Tablette(n)A07EC0204.09.0.B

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Yaldigo 400 mg authorised in Switzerland?

Yes. Yaldigo 400 mg is authorised by Swissmedic under authorisation number 53108, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Yaldigo 400 mg have?

Yaldigo 400 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 Yaldigo 400 mg?

The authorisation holder is Tillotts Pharma 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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