MedPath

LUNDIRAN 250 mg Cápsulas duras

LUNDIRAN 250 mg Cápsulas duras

Commercialized
Register Number

54246

Prescription Type

Medicamento Sujeto A Prescripción Médica

Authorization Date

Jun 30, 1977

Dosage Form

CÁPSULA DURA

Route: VÍA ORAL

Product Details

Detailed information about this CIMA AEMPS approved pharmaceutical product.

Basic Information

Key regulatory and product classification details

Regulatory Details

Register Number54246
EMA Approved
No

Drug Classification

Generic
No
Orphan
No
Biosimilar
No
Commercialized
Yes
CIMA AEMPS Classification

INGREDIENTS (1)

NAPROXENOActive
Quantity: 250 mg
Name: NAPROXENO

ATC CLASSIFICATION (3)

M01A
M01AE
M01AE02

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.