PRODUCT DETAIL

Ibuprofen Dr.Max 20 mg/ml perorálna suspenzia

Code

9392D

MA number

07/0002/22-S

Product Form:

sus por1x100 ml/2000 mg (fľ.skl.hnedá+PP uzáver s bezpeč.kruž.+striekačka)

MA Status:

R - Valid Marketing Authorisation

Type of procedure:

Mutual recognition procedure

Therapeutic Class:

07 - ANALGETICA, ANTIPYRETICA

ATC:

M	MUSCULO-SKELETAL SYSTEM
M01	ANTIINFLAMMATORY AND ANTIRHEUMATIC PRODUCTS
M01A	ANTIINFLAMMATORY AND ANTIRHEUMATIC PRODUCTS, NON-S
M01AE	Propionic acid derivatives
M01AE01	Ibuprofen

Shelf life:

Container:

brown glass bottle

Route of admin.:

Oral use

Prescription Status:	Medicinal product not subject to medical prescription.
Legal basis:	Article 10(1) generic application
MA issued:	29.01.2022
Validity:	29.01.2027
Pediatric indication:	Yes
Pediatric posology:	Yes
Pediatric warnings:	Yes
SPC:	SPC_Ibuprofen Dr.Max 20 mg-ml perorálna suspenzia_04.2024.pdf
PIL:	PIL_Ibuprofen Dr.Max 20 mg-ml perorálna suspenzia_04.2024.pdf
Safety feature	No
Data update:	01.02.2022