Puregon 300 I.E.

Puregon 300 I.E. is a medicine authorised by Swissmedic under authorisation number 55453. The authorisation holder is Organon GmbH. The medicinal product code is Biotechnological 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 14 June 2001 and the authorisation is valid without a time limit. ATC code G03GA06 places the medicine in the group Sex hormones and modulators of the genital system.

Dispensing category A
Authorisation number 55453
ATC G03GA06
Biotechnological medicines

Authorisation data
Authorisation number	55453
Name	Puregon 300 I.E.
Full name	Puregon 300 I.E., Injektionslösung in einer Patrone
Authorisation holder	Organon GmbH
Medicinal product code	Biotechnological medicines
Dispensing category	A · Prescription, not repeatable
ATC code	G03GA06
First authorisation	14 June 2001
Authorisation validity	unlimited

Strengths
No.	Name	Dispensing category	Authorisation date
1	Puregon 300 I.E., Injektionslösung in einer Patrone	A	14 June 2001
2	Puregon 600 I.E., Injektionslösung in einer Patrone	A	14 June 2001
4	Puregon 900 I.E., Injektionslösung in einer Patrone	A	08 November 2005

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Pack sizes
Pack code	Quantity	Unit	ATC	IT code	Dispensing category
2	1	Patrone	G03GA06	07.08.1.	A
4	1	Patrone	G03GA06	07.08.1.	A
6	1	Patrone	G03GA06	07.08.1.	A

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Other medicines from this authorisation holder

AeriusAuthorisation number 55689 · ATC R06AX27D AeriusAuthorisation number 55958 · ATC R06AX27B Arcoxia 30 mgAuthorisation number 56079 · ATC M01AH05B Atozet 10 mg / 10 mgAuthorisation number 65223 · ATC C10BA05B CerazetteAuthorisation number 55155 · ATC G03AC09B CircletAuthorisation number 66498 · ATC G02BB01B Cosaar 50Authorisation number 52904 · ATC C09CA01B Cosaar Plus 50/12.5Authorisation number 53629 · ATC C09DA01B

Frequently asked questions

Is Puregon 300 I.E. authorised in Switzerland?

Yes. Puregon 300 I.E. is authorised by Swissmedic under authorisation number 55453, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Puregon 300 I.E. have?

Puregon 300 I.E. 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 Puregon 300 I.E.?

The authorisation holder is Organon GmbH. 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.