Sifrol ER 0

Sifrol ER 0 is a medicine authorised by Swissmedic under authorisation number 60057. The authorisation holder is Boehringer Ingelheim (Schweiz) GmbH. 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 10 June 2010 and the authorisation is valid without a time limit. ATC code N04BC05 places the medicine in the group Anti-Parkinson drugs.

  • Dispensing category B
  • Authorisation number 60057
  • ATC N04BC05
  • Synthetic medicines
Authorisation data
Authorisation number60057
NameSifrol ER 0
Full nameSifrol ER 0,375 mg, Retardtabletten
Authorisation holderBoehringer Ingelheim (Schweiz) GmbH
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeN04BC05
First authorisation10 June 2010
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Sifrol ER 0,375 mg, RetardtablettenB10 June 2010
2Sifrol ER 0,75 mg, RetardtablettenB10 June 2010
3Sifrol ER 1,5 mg, RetardtablettenB10 June 2010
4Sifrol ER 3,0 mg, RetardtablettenB10 June 2010
5Sifrol ER 4,5 mg, RetardtablettenB10 June 2010

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
110Tablette(n)N04BC0501.08.0.B
210Tablette(n)N04BC0501.08.0.B
330Tablette(n)N04BC0501.08.0.B
430Tablette(n)N04BC0501.08.0.B
530Tablette(n)N04BC0501.08.0.B
630Tablette(n)N04BC0501.08.0.B

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Sifrol ER 0 authorised in Switzerland?

Yes. Sifrol ER 0 is authorised by Swissmedic under authorisation number 60057, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Sifrol ER 0 have?

Sifrol ER 0 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 Sifrol ER 0?

The authorisation holder is Boehringer Ingelheim (Schweiz) GmbH. 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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