ROPINIROLE EG LP 8 mg, extended-release film-coated tablet 28 tablets
Active ingredients: Ropinirole hydrochloride, Ropinirol
Commercialized according to BDPMANSM noticeDispensing in France: Prescription only
Extended-release film-coated tablet28 tabletsorale
Supply disruption
Package details
Original BDPM fields are shown in French.
- Official name
- ROPINIROLE EG LP 8 mg, comprimé pelliculé à libération prolongée
- Pharmaceutical form
- comprimé pelliculé à libération prolongée
- Route of administration
- orale
- Presentation description
- plaquette(s) PVC polychlortrifluoroéthylène aluminium de 28 comprimé(s)
- Marketing authorisation holder
- EG LABO - LABORATOIRES EUROGENERICS
- Reimbursement according to BDPM
- 65%
- Approval for use in healthcare institutions
- oui
- Commercialization declaration date
- 7 Feb 2013
- Prescription and dispensing conditions
- Prescription only
- List I: prescription-only medicine
- Enhanced ANSM monitoring
- No
BDPM identifiers
CIS
60274618CIP72235859CIP133400922358598Composition in BDPM
| Component | Amount per unit | Source type |
|---|---|---|
| CHLORHYDRATE DE ROPINIROLEcomprimé | — | SA |
| ROPINIROLEcomprimé | 8 mg · un comprimé | FT |
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.