PUREGON 900 IU/1.08 ml, solution for injection cartridge, 1.23 ml
Active ingredients: FOLLITROPINE BÊTA
Commercialized according to BDPMDispensing in France: Prescription only
Solution for injectioncartridge, 1.23 mlsous-cutanée
No current ANSM shortage notice is included
Package details
Original BDPM fields are shown in French.
- Official name
- PUREGON 900 UI/1,08 ml, solution injectable
- Pharmaceutical form
- solution injectable
- Route of administration
- sous-cutanée
- Presentation description
- 1 cartouche(s) en verre de 1,23 ml avec 9 aiguille(s)
- Marketing authorisation holder
- ORGANON (HOLLANDE)
- Reimbursement according to BDPM
- 100%
- Approval for use in healthcare institutions
- oui
- Commercialization declaration date
- 20 Apr 2005
- Prescription and dispensing conditions
- Prescription only
- List I: prescription-only medicine
- Requires special monitoring during treatment
- Prescribed by specialists only
- Enhanced ANSM monitoring
- No
BDPM identifiers
CIS
60727755CIP73651413CIP133400936514133Composition in BDPM
| Component | Amount per unit | Source type |
|---|---|---|
| FOLLITROPINE BÊTAsolution | 1025 UI · une cartouche | SA |
Information is based on BDPM data and is for reference only. Consult a doctor before use.
Other packages of this medicine
The same medicine in another pack size, according to BDPM.
Similar medicines
Similar medicines are listed using the official BDPM catalog. Availability must be checked separately. Consult a doctor or pharmacist before switching medicines.
The current BDPM data does not list similar medicines for this product.