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Approvals
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CIMA-AEMPS
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CYMBALTA 30 MG CAPSULAS DURAS GASTRORRESISTENTES
Approved
STANDARD
CYMBALTA 30 MG CAPSULAS DURAS GASTRORRESISTENTES
Eli Lilly Nederland B.V.
🇪🇸 Spanish Agency of Medicines and Medical Devices
Approval Date
Dec 14, 2021
Approval ID
68f7e874d9db9877
Company
Eli Lilly Nederland B.V.
Type
Standard
Approval Details
Approval Id
68f7e874d9db9877
Drug Cima Aemps Name
CYMBALTA 30 MG CAPSULAS DURAS GASTRORRESISTENTES
Register Number
04296001IP1
Holder Company Name
Eli Lilly Nederland B.V.
Marketing Company Name
Ecofar Productos S.L.
Holder Company Detail Path
/organization/eli-lilly-nederland-bv
Authorization Date
2021-12-14
Dosage Form
CÁPSULA DURA GASTRORRESISTENTE
Dose
30 mg
Route Of Administration
VÍA ORAL
Prescription Type
Medicamento Sujeto A Prescripción Médica
Commercialized
Yes
Company Name
Eli Lilly Nederland B.V.
Company Detail Path
/organization/eli-lilly-nederland-bv
Company Information
Pharmaceutical Company Name
Eli Lilly Nederland BV
Country Name
Netherlands
Website
http://www.lilly.com/nl
Active Ingredients
DULOXETINA HIDROCLORURO
30 mg
Approved
Quick Info
Agency
CIMA-AEMPS
Country
🇪🇸
Approval Date
Dec 14, 2021
Approval ID
68f7e874d9db9877
Type
Standard
Back to CIMA-AEMPS Approvals
CYMBALTA 30 MG CAPSULAS DURAS GASTRORRESISTENTES - CIMA-AEMPS Drug Approval Details