Uptravi 200 mcg

Uptravi 200 mcg is a medicine authorised by Swissmedic under authorisation number 65643. The authorisation holder is Janssen-Cilag 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 August 2016 and the authorisation is valid without a time limit. ATC code B01AC27 places the medicine in the group Antithrombotic agents.

  • Dispensing category B
  • Authorisation number 65643
  • ATC B01AC27
  • Synthetic medicines
Authorisation data
Authorisation number65643
NameUptravi 200 mcg
Full nameUptravi 200 mcg, Filmtabletten
Authorisation holderJanssen-Cilag AG
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeB01AC27
First authorisation15 August 2016
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Uptravi 200 mcg, FilmtablettenB15 August 2016
2Uptravi 400 mcg, FilmtablettenB15 August 2016
3Uptravi 600 mcg, FilmtablettenB15 August 2016
4Uptravi 800 mcg, FilmtablettenB15 August 2016
5Uptravi 1000 mcg, FilmtablettenB15 August 2016
6Uptravi 1200 mcg, FilmtablettenB15 August 2016
7Uptravi 1400 mcg, FilmtablettenB15 August 2016
8Uptravi 1600 mcg, FilmtablettenB15 August 2016

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
160Tablette(n)B01AC2702.07.1.B
2140Tablette(n)B01AC2702.07.1.B
360Tablette(n)B01AC2702.07.1.B
460Tablette(n)B01AC2702.07.1.B
560Tablette(n)B01AC2702.07.1.B
660Tablette(n)B01AC2702.07.1.B
760Tablette(n)B01AC2702.07.1.B
860Tablette(n)B01AC2702.07.1.B
960Tablette(n)B01AC2702.07.1.B

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Other medicines from this authorisation holder

Frequently asked questions

Is Uptravi 200 mcg authorised in Switzerland?

Yes. Uptravi 200 mcg is authorised by Swissmedic under authorisation number 65643, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Uptravi 200 mcg have?

Uptravi 200 mcg 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 Uptravi 200 mcg?

The authorisation holder is Janssen-Cilag 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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