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Approvals
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CIMA-AEMPS
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AZACITIDINA HIKMA 25 MG/ML POLVO PARA SUSPENSION INYECTABLE EFG
Approved
STANDARD
AZACITIDINA HIKMA 25 MG/ML POLVO PARA SUSPENSION INYECTABLE EFG
Hikma Farmaceutica (Portugal) S.A.
🇪🇸 Spanish Agency of Medicines and Medical Devices
Approval Date
Dec 9, 2022
Approval ID
d535e3a243e50a5b
Company
Hikma Farmaceutica (Portugal) S.A.
Type
Standard
Approval Details
Approval Id
d535e3a243e50a5b
Drug Cima Aemps Name
AZACITIDINA HIKMA 25 MG/ML POLVO PARA SUSPENSION INYECTABLE EFG
Register Number
87680
Holder Company Name
Hikma Farmaceutica (Portugal) S.A.
Marketing Company Name
Hikma España, S.L.U.
Holder Company Detail Path
/organization/hikma-farmaceutica-portugal-s-a
Authorization Date
2022-12-09
Dosage Form
POLVO PARA SUSPENSIÓN INYECTABLE
Dose
25 mg/ml
Route Of Administration
VÍA SUBCUTÁNEA
Prescription Type
Uso Hospitalario
Commercialized
Yes
Company Name
Hikma Farmaceutica (Portugal) S.A.
Company Detail Path
/organization/hikma-farmaceutica-portugal-s-a
Company Information
Pharmaceutical Company Name
HIKMA FARMACÊUTICA (PORTUGAL), S.A.
Country Name
Portugal
City Name
terrugem snt,lisboa,country_pt
Address
ESTRADA RIO DA MÓ, 8/8A/B
Active Ingredients
AZACITIDINA
25 mg/ml
Approved
Quick Info
Agency
CIMA-AEMPS
Country
🇪🇸
Approval Date
Dec 9, 2022
Approval ID
d535e3a243e50a5b
Type
Standard
Back to CIMA-AEMPS Approvals
AZACITIDINA HIKMA 25 MG/ML POLVO PARA SUSPENSION INYECTABLE EFG - CIMA-AEMPS Drug Approval Details
