Bactroban Nasal

Bactroban Nasal is a medicine authorised by Swissmedic under authorisation number 52361. The authorisation holder is GlaxoSmithKline AG. The medicinal product code is Synthetic medicines and the dispensing category is A: Supplied only against a medical or veterinary prescription that may not be dispensed repeatedly. First authorisation was granted on 28 January 1994 and the authorisation is valid without a time limit. ATC code R01AX06 places the medicine in the group Nasal preparations.

  • Dispensing category A
  • Authorisation number 52361
  • ATC R01AX06
  • Synthetic medicines
Authorisation data
Authorisation number52361
NameBactroban Nasal
Full nameBactroban Nasal, Nasensalbe
Authorisation holderGlaxoSmithKline AG
Medicinal product codeSynthetic medicines
Dispensing categoryA · Prescription, not repeatable
ATC codeR01AX06
First authorisation28 January 1994
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Bactroban Nasal, NasensalbeA28 January 1994

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
283gR01AX0612.02.51A

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Other medicines from this authorisation holder

Frequently asked questions

Is Bactroban Nasal authorised in Switzerland?

Yes. Bactroban Nasal is authorised by Swissmedic under authorisation number 52361, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Bactroban Nasal have?

Bactroban Nasal is in dispensing category A. Supplied only against a medical or veterinary prescription that may not be dispensed repeatedly.

Who is the authorisation holder of Bactroban Nasal?

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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