Ferinject 1000 mg / 20 ml

Ferinject 1000 mg / 20 ml is a medicine authorised by Swissmedic under authorisation number 70544. The authorisation holder is EurimPharm Swiss 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 17 March 2026 and the authorisation is limited until 16 March 2031. ATC code B03AC places the medicine in the group Antianemic preparations.

  • Dispensing category B
  • Authorisation number 70544
  • ATC B03AC
  • Synthetic medicines
Authorisation data
Authorisation number70544
NameFerinject 1000 mg / 20 ml
Full nameFerinject 1000 mg / 20 ml, Dispersion zur Injektion/Infusion
Authorisation holderEurimPharm Swiss AG
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeB03AC
First authorisation17 March 2026
Authorisation validity16 March 2031
Strengths
No.NameDispensing categoryAuthorisation date
1Ferinject 1000 mg / 20 ml, Dispersion zur Injektion/InfusionB17 March 2026
2Ferinject 500 mg / 10 ml, Dispersion zur Injektion/InfusionB17 March 2026

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
31 x 20 mlDurchstechflasche(n)B03AC06.07.1.B
11 x 10 mlDurchstechflasche(n)B03AC06.07.1.B
25 x 10 mlDurchstechflasche(n)B03AC06.07.1.B

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Ferinject 1000 mg / 20 ml authorised in Switzerland?

Yes. Ferinject 1000 mg / 20 ml is authorised by Swissmedic under authorisation number 70544, data as of 01 September 2026. The authorisation is limited until 16 March 2031.

Which dispensing category does Ferinject 1000 mg / 20 ml have?

Ferinject 1000 mg / 20 ml 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 Ferinject 1000 mg / 20 ml?

The authorisation holder is EurimPharm Swiss 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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