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KYNMOBI 15 MG PELÍCULA SUBLINGUAL - CIMA-AEMPS Drug Approval Details

Approvals/CIMA-AEMPS/KYNMOBI 15 MG PELÍCULA SUBLINGUAL

Approved

STANDARD

KYNMOBI 15 MG PELÍCULA SUBLINGUAL

Bial Portela & Ca S.A.🇪🇸 Spanish Agency of Medicines and Medical Devices

Approval Date: Dec 5, 2023
Approval ID: a03d586193c3f55f
Company: Bial Portela & Ca S.A.
Type: Standard

Approval Details

Approval Id: a03d586193c3f55f
Drug Cima Aemps Name: KYNMOBI 15 MG PELÍCULA SUBLINGUAL
Register Number: 88977
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: 15 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 HEMIHIDRATO

15 mg

Approved

Quick Info

Agency

CIMA-AEMPS

Country

🇪🇸

Approval Date

Dec 5, 2023

Approval ID

a03d586193c3f55f

Type

Standard

Back to CIMA-AEMPS Approvals