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FENISTIL 1 MG/ML EMULSION CUTANEA - CIMA-AEMPS Drug Approval Details
Approvals
/
CIMA-AEMPS
/
FENISTIL 1 MG/ML EMULSION CUTANEA
Approved
STANDARD
FENISTIL 1 MG/ML EMULSION CUTANEA
Glaxosmithkline Consumer Healthcare Hellas S.A.
🇪🇸 Spanish Agency of Medicines and Medical Devices
Approval Date
Jul 6, 2020
Approval ID
08d079b341428814
Company
Glaxosmithkline Consumer Healthcare Hellas S.A.
Type
Standard
Approval Details
Approval Id
08d079b341428814
Drug Cima Aemps Name
FENISTIL 1 MG/ML EMULSION CUTANEA
Register Number
37189-7-6-2010
Holder Company Name
Glaxosmithkline Consumer Healthcare Hellas S.A.
Marketing Company Name
Difarmed S.L.U.
Authorization Date
2020-07-06
Dosage Form
EMULSIÓN CUTÁNEA
Dose
1 mg
Route Of Administration
USO CUTÁNEO
Prescription Type
Sin Receta
Commercialized
Yes
Company Name
Glaxosmithkline Consumer Healthcare Hellas S.A.
Active Ingredients
DIMETINDENO MALEATO
1 mg
Approved
Quick Info
Agency
CIMA-AEMPS
Country
🇪🇸
Approval Date
Jul 6, 2020
Approval ID
08d079b341428814
Type
Standard
Back to CIMA-AEMPS Approvals