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Approvals
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CIMA-AEMPS
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AZUL PATENTE AZULTIS 25 MG/ML SOLUCION INYECTABLE EFG
Approved
STANDARD
AZUL PATENTE AZULTIS 25 MG/ML SOLUCION INYECTABLE EFG
Provepharm
🇪🇸 Spanish Agency of Medicines and Medical Devices
Approval Date
Oct 6, 2025
Approval ID
890c113ecba5066a
Company
Provepharm
Type
Standard
Approval Details
Approval Id
890c113ecba5066a
Drug Cima Aemps Name
AZUL PATENTE AZULTIS 25 MG/ML SOLUCION INYECTABLE EFG
Register Number
90644
Holder Company Name
Provepharm
Marketing Company Name
Provepharm
Authorization Date
2025-10-06
Dosage Form
SOLUCIÓN INYECTABLE
Dose
25 mg/ml
Route Of Administration
VÍA INTRAARTERIAL, VÍA SUBCUTÁNEA
Prescription Type
Uso Hospitalario
Commercialized
No
Company Name
Provepharm
Approved
Quick Info
Agency
CIMA-AEMPS
Country
🇪🇸
Approval Date
Oct 6, 2025
Approval ID
890c113ecba5066a
Type
Standard
Back to CIMA-AEMPS Approvals
AZUL PATENTE AZULTIS 25 MG/ML SOLUCION INYECTABLE EFG - CIMA-AEMPS Drug Approval Details
