AZACITIDINE HIKMA 25 mg/ml, powder for injectable suspension bottle
Active ingredients: Azacitidine
Commercialized according to BDPMDispensing in France: Prescription only
Powder for injectable suspensionbottlesous-cutanée
No current ANSM shortage notice is included
Package details
Original BDPM fields are shown in French.
- Official name
- AZACITIDINE HIKMA 25 mg/mL, poudre pour suspension injectable
- Pharmaceutical form
- poudre pour suspension injectable
- Route of administration
- sous-cutanée
- Presentation description
- 1 flacon(s) en verre de 100 mg
- Marketing authorisation holder
- HIKMA FARMACEUTICA (PORTUGAL)
- Reimbursement according to BDPM
- —
- Approval for use in healthcare institutions
- oui
- Commercialization declaration date
- 31 May 2024
- Prescription and dispensing conditions
- Prescription only
- List I: prescription-only medicine
- Requires special monitoring during treatment
- Prescribed by a hospital doctor
- Prescribed by specialists only
- Enhanced ANSM monitoring
- No
BDPM identifiers
CIS
61118013CIP73025677CIP133400930256770Composition in BDPM
| Component | Amount per unit | Source type |
|---|---|---|
| AZACITIDINEpoudre | 100 mg · un flacon | 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.