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OLMESARTAN/AMLODIPINO/HIDROCLOROTIAZIDA LACER 20 MG/5 MG/12,5 MG COMPRIMIDOS RECUBIERTOS CON PELICULA EFG - CIMA-AEMPS Drug Approval Details
Approvals
/
CIMA-AEMPS
/
OLMESARTAN/AMLODIPINO/HIDROCLOROTIAZIDA LACER 20 MG/5 MG/12,5 MG COMPRIMIDOS RECUBIERTOS CON PELICULA EFG
Approved
STANDARD
OLMESARTAN/AMLODIPINO/HIDROCLOROTIAZIDA LACER 20 MG/5 MG/12,5 MG COMPRIMIDOS RECUBIERTOS CON PELICULA EFG
Lacer S.A.
🇪🇸 Spanish Agency of Medicines and Medical Devices
Approval Date
Dec 9, 2020
Approval ID
c853aead22889289
Company
Lacer S.A.
Type
Standard
Approval Details
Approval Id
c853aead22889289
Drug Cima Aemps Name
OLMESARTAN/AMLODIPINO/HIDROCLOROTIAZIDA LACER 20 MG/5 MG/12,5 MG COMPRIMIDOS RECUBIERTOS CON PELICULA EFG
Register Number
85635
Holder Company Name
Lacer S.A.
Marketing Company Name
Lacer S.A.
Authorization Date
2020-12-09
Dosage Form
COMPRIMIDO RECUBIERTO CON PELÍCULA
Dose
20 mg/5 mg/12,5 mg
Route Of Administration
VÍA ORAL
Prescription Type
Medicamento Sujeto A Prescripción Médica
Commercialized
No
Company Name
Lacer S.A.
Active Ingredients
OLMESARTAN MEDOXOMILO
20 mg
AMLODIPINO BESILATO
6,93 mg
HIDROCLOROTIAZIDA
12,5 mg
Approved
Quick Info
Agency
CIMA-AEMPS
Country
🇪🇸
Approval Date
Dec 9, 2020
Approval ID
c853aead22889289
Type
Standard
Back to CIMA-AEMPS Approvals