PRAMIPEXOLE ZENTIVA LP 0.26 mg, extended-release tablet 30 tablets
Active ingredients: Pramipexole dihydrochloride hydrate, Pramipexole
Commercialized according to BDPMDispensing in France: Prescription only
Extended-release tablet30 tabletsorale
No current ANSM shortage notice is included
Package details
Original BDPM fields are shown in French.
- Official name
- PRAMIPEXOLE ZENTIVA LP 0,26 mg, comprimé à libération prolongée
- Pharmaceutical form
- comprimé à libération prolongée
- Route of administration
- orale
- Presentation description
- plaquette(s) aluminium OPA : polyamide orienté PVC de 30 comprimé(s)
- Marketing authorisation holder
- ZENTIVA FRANCE
- Reimbursement according to BDPM
- 65%
- Approval for use in healthcare institutions
- oui
- Commercialization declaration date
- 6 Jun 2018
- Prescription and dispensing conditions
- Prescription only
- List I: prescription-only medicine
- Enhanced ANSM monitoring
- No
BDPM identifiers
CIS
64487282CIP73010989CIP133400930109892Composition in BDPM
| Component | Amount per unit | Source type |
|---|---|---|
| DICHLORHYDRATE DE PRAMIPEXOLE MONOHYDRATÉcomprimé | 0,375 mg · un comprimé | SA |
| PRAMIPEXOLEcomprimé | 0,26 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.