
PUREGON 600 IU/0.72 ml, solution for injection cartridge, 0.84 ml
Active ingredients: FOLLITROPINE BÊTA
Commercialized according to BDPMDispensing in France: Prescription only
Solution for injectioncartridge, 0.84 mlsous-cutanée
No current ANSM shortage notice is included
Package details
Original BDPM fields are shown in French.
- Official name
- PUREGON 600 UI/0,72 ml, solution injectable
- Pharmaceutical form
- solution injectable
- Route of administration
- sous-cutanée
- Presentation description
- 1 cartouche(s) en verre de 0,84 ml avec 6 aiguille(s)
- Marketing authorisation holder
- ORGANON (HOLLANDE)
- Reimbursement according to BDPM
- 100%
- Approval for use in healthcare institutions
- oui
- Commercialization declaration date
- 24 Apr 2002
- 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
65214799CIP73530980CIP133400935309808Composition in BDPM
| Component | Amount per unit | Source type |
|---|---|---|
| FOLLITROPINE BÊTAsolution | 700 UI · une cartouche | SA |
Information is based on BDPM data and is for reference only. Consult a doctor before use.
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.