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KYNMOBI 20 MG PELÍCULA SUBLINGUAL - CIMA-AEMPS Drug Approval Details
Approvals
/
CIMA-AEMPS
/
KYNMOBI 20 MG PELÍCULA SUBLINGUAL
Approved
STANDARD
KYNMOBI 20 MG PELÍCULA SUBLINGUAL
Bial Portela & Ca S.A.
🇪🇸 Spanish Agency of Medicines and Medical Devices
Approval Date
Dec 5, 2023
Approval ID
b132b30381345873
Company
Bial Portela & Ca S.A.
Type
Standard
Approval Details
Approval Id
b132b30381345873
Drug Cima Aemps Name
KYNMOBI 20 MG PELÍCULA SUBLINGUAL
Register Number
88978
Holder Company Name
Bial Portela & Ca S.A.
Marketing Company Name
Laboratorios Bial S.A.
Holder Company Detail Path
/organization/bial-portela-and-ca-s-a
Authorization Date
2023-12-05
Dosage Form
PELICULA SUBLINGUAL
Dose
20 mg
Route Of Administration
VÍA SUBLINGUAL
Prescription Type
Diagnóstico Hospitalario
Commercialized
Yes
Company Name
Bial Portela & Ca S.A.
Company Detail Path
/organization/bial-portela-and-ca-s-a
Company Information
Pharmaceutical Company Name
BIAL - PORTELA & CA., S.A.
Country Name
Portugal
City Name
são mamede coronado,porto,country_pt
Address
AVENIDA DA SIDERÚRGIA NACIONAL
Active Ingredients
APOMORFINA HIDROCLORURO
20 mg
Approved
Quick Info
Agency
CIMA-AEMPS
Country
🇪🇸
Approval Date
Dec 5, 2023
Approval ID
b132b30381345873
Type
Standard
Back to CIMA-AEMPS Approvals