Requip-Modutab 2 mg

Requip-Modutab 2 mg is a medicine authorised by Swissmedic under authorisation number 57740. The authorisation holder is GlaxoSmithKline 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 06 November 2007 and the authorisation is valid without a time limit. ATC code N04BC04 places the medicine in the group Anti-Parkinson drugs.

  • Dispensing category B
  • Authorisation number 57740
  • ATC N04BC04
  • Synthetic medicines
Authorisation data
Authorisation number57740
NameRequip-Modutab 2 mg
Full nameRequip-Modutab 2 mg, Tabletten mit veränderter Wirkstofffreisetzung
Authorisation holderGlaxoSmithKline AG
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeN04BC04
First authorisation06 November 2007
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Requip-Modutab 2 mg, Tabletten mit veränderter WirkstofffreisetzungB06 November 2007
3Requip-Modutab 4 mg, Tabletten mit veränderter WirkstofffreisetzungB06 November 2007
4Requip-Modutab 8 mg, Tabletten mit veränderter WirkstofffreisetzungB06 November 2007

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
328Tablette(n)N04BC0401.08.0.B
1128Tablette(n)N04BC0401.08.0.B
1528Tablette(n)N04BC0401.08.0.B

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Requip-Modutab 2 mg authorised in Switzerland?

Yes. Requip-Modutab 2 mg is authorised by Swissmedic under authorisation number 57740, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Requip-Modutab 2 mg have?

Requip-Modutab 2 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 Requip-Modutab 2 mg?

The authorisation holder is GlaxoSmithKline 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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