Erythromycine Panpharma 500 mg

Erythromycine Panpharma 500 mg is a medicine authorised by Swissmedic under authorisation number 70183. The authorisation holder is Leman SKL SA. 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 26 March 2026 and the authorisation is limited until 25 March 2031. ATC code J01FA01 places the medicine in the group Antibacterials for systemic use.

  • Dispensing category A
  • Authorisation number 70183
  • ATC J01FA01
  • Synthetic medicines
Authorisation data
Authorisation number70183
NameErythromycine Panpharma 500 mg
Full nameErythromycine Panpharma 500 mg, poudre pour solution à diluer pour perfusion
Authorisation holderLeman SKL SA
Medicinal product codeSynthetic medicines
Dispensing categoryA · Prescription, not repeatable
ATC codeJ01FA01
First authorisation26 March 2026
Authorisation validity25 March 2031
Strengths
No.NameDispensing categoryAuthorisation date
1Erythromycine Panpharma 500 mg, poudre pour solution à diluer pour perfusionA26 March 2026
2Erythromycine Panpharma 1 g, poudre pour solution à diluer pour perfusionA26 March 2026

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
110Ampulle(n)J01FA0108.01.6.A
210Ampulle(n)J01FA0108.01.6.A

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Erythromycine Panpharma 500 mg authorised in Switzerland?

Yes. Erythromycine Panpharma 500 mg is authorised by Swissmedic under authorisation number 70183, data as of 01 September 2026. The authorisation is limited until 25 March 2031.

Which dispensing category does Erythromycine Panpharma 500 mg have?

Erythromycine Panpharma 500 mg 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 Erythromycine Panpharma 500 mg?

The authorisation holder is Leman SKL SA. 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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