Floxapen 500 mg i.v./i.m.

Floxapen 500 mg i.v./i.m. is a medicine authorised by Swissmedic under authorisation number 37404. The authorisation holder is Teva Pharma 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 16 November 1972 and the authorisation is valid without a time limit. ATC code J01CF05 places the medicine in the group Antibacterials for systemic use.

  • Dispensing category B
  • Authorisation number 37404
  • ATC J01CF05
  • Synthetic medicines
Authorisation data
Authorisation number37404
NameFloxapen 500 mg i.v./i.m.
Full nameFloxapen 500 mg i.v./i.m., Pulver zur Herstellung einer Injektions-/Infusionslösung
Authorisation holderTeva Pharma AG
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeJ01CF05
First authorisation16 November 1972
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
2Floxapen 500 mg i.v./i.m., Pulver zur Herstellung einer Injektions-/InfusionslösungB16 November 1972
3Floxapen 1 g i.v./i.m., Pulver zur Herstellung einer Injektions-/InfusionslösungB16 November 1972
4Floxapen 2 g i.v., Pulver zur Herstellung einer Injektions-/InfusionslösungB11 April 2012

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
2010Durchstechflasche(n)J01CF0508.01.24B
3910Durchstechflasche(n)J01CF0508.01.24B
4010Durchstechflasche(n)J01CF0508.01.24B

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Floxapen 500 mg i.v./i.m. authorised in Switzerland?

Yes. Floxapen 500 mg i.v./i.m. is authorised by Swissmedic under authorisation number 37404, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Floxapen 500 mg i.v./i.m. have?

Floxapen 500 mg i.v./i.m. 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 Floxapen 500 mg i.v./i.m.?

The authorisation holder is Teva Pharma 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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