Dekristol 20.000 I.E.

Dekristol 20.000 I.E. is a medicine authorised by Swissmedic under authorisation number 68261. The authorisation holder is Dermapharm 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 25 May 2023 and the authorisation is limited until 24 May 2028. ATC code A11CC05 places the medicine in the group Vitamins.

Dispensing category B
Authorisation number 68261
ATC A11CC05
Synthetic medicines

Authorisation data
Authorisation number	68261
Name	Dekristol 20.000 I.E.
Full name	Dekristol 20.000 I.E., Weichkapseln
Authorisation holder	Dermapharm AG
Medicinal product code	Synthetic medicines
Dispensing category	B · Prescription only
ATC code	A11CC05
First authorisation	25 May 2023
Authorisation validity	24 May 2028

Strengths
No.	Name	Dispensing category	Authorisation date
1	Dekristol 20.000 I.E., Weichkapseln	B	25 May 2023

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Pack sizes
Pack code	Quantity	Unit	ATC	IT code	Dispensing category
1	14	Kapsel(n)	A11CC05	07.02.3.	B
2	3	Kapsel(n)	A11CC05	07.02.3.	B
3	4	Kapsel(n)	A11CC05	07.02.3.	B
4	6	Kapsel(n)	A11CC05	07.02.3.	B
5	14	Kapsel(n)	A11CC05	07.02.3.	B
6	50	Kapsel(n)	A11CC05	07.02.3.	B

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Medicines in the same ATC group

D3 VitaCaps 24Authorisation number 68197 · Pierre Fabre Pharma SA · ATC A11CC05B DIBASE 10'000Authorisation number 65856 · EffRx Pharmaceuticals SA · ATC A11CC05D DIBASE 25'000Authorisation number 65857 · EffRx Pharmaceuticals SA · ATC A11CC05B/D HEMONITA D3 zur ProphylaxeAuthorisation number 66441 · Hemony Pharmaceutical Switzerland GmbH · ATC A11CC05B/D LundeosAuthorisation number 67796 · Labatec Pharma SA · ATC A11CC05B Luvit D3 zur ProphylaxeAuthorisation number 66124 · Drossapharm AG · ATC A11CC05B/D Trederol 20000 I.E.Authorisation number 69041 · Biomed AG · ATC A11CC05B Veractiv Vitamin D3 Wild HuileAuthorisation number 57690 · Verfora SA · ATC A11CC05D Vi-De 3Authorisation number 9395 · Verfora SA · ATC A11CC05D Vi-De 3 Huile 0.5 mg/mlAuthorisation number 65400 · Verfora SA · ATC A11CC05D Vi-De 3 capsules 5600 U.I.Authorisation number 70409 · Verfora SA · ATC A11CC05B Vi-De 3 capsules 800 U.I.Authorisation number 70395 · Verfora SA · ATC A11CC05D

Other medicines from this authorisation holder

Acicutan 10 mgAuthorisation number 61876 · ATC D05BB02A AdabencutanAuthorisation number 70282 · ATC D10AD53B Alitrecutan 10 mgAuthorisation number 68818 · ATC D11AH04A Allergovit Alnus KombipackungAuthorisation number 60633 · ATC V01AAA Allergovit Alnus/Corylus KombipackungAuthorisation number 60624 · ATC V01AAA Allergovit Artemisia KombipackungAuthorisation number 60641 · ATC V01AAA Allergovit Betula KombipackungAuthorisation number 60642 · ATC V01AAA Allergovit Betula/Alnus/Corylus KombipackungAuthorisation number 60636 · ATC V01AAA

Frequently asked questions

Is Dekristol 20.000 I.E. authorised in Switzerland?

Yes. Dekristol 20.000 I.E. is authorised by Swissmedic under authorisation number 68261, data as of 01 September 2026. The authorisation is limited until 24 May 2028.

Which dispensing category does Dekristol 20.000 I.E. have?

Dekristol 20.000 I.E. 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 Dekristol 20.000 I.E.?

The authorisation holder is Dermapharm 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.