PRODUCT DETAIL

Dehorsan 500 mg/200 mg/4 mg šumivý granulát

Code

4031E

MA number

07/0177/23-S

Product Form:

gra eff 20x500 mg/200 mg/4 mg (vre.papier/Al/PE)

MA Status:

R - Valid Marketing Authorisation

Type of procedure:

Decentralised

MAH, country:

Natur Produkt Zdrovit Sp. z o.o., Poland

Therapeutic Class:

07 - ANALGETICA, ANTIPYRETICA

ATC:

N	NERVOUS SYSTEM
N02	ANALGESICS
N02B	OTHER ANALGESICS AND ANTIPYRETICS
N02BE	Anilides
N02BE51	Paracetamol, combinations excluding psycholeptics

Shelf life:

Container:

sachet paper/Al/PE

Route of admin.:

Oral use

Prescription Status:	Medicinal product not subject to medical prescription.
Legal basis:	Article 10a well-established use application
MA issued:	11.08.2023
Validity:	11.08.2028
Pediatric indication:	Yes
Pediatric posology:	Yes
Pediatric contraindication:	Yes
Pediatric warnings:	Yes
SPC:	SPC_Dehorsan 500 mg-200 mg-4 mg šumivý granulát_08.2025.pdf
PIL:	PIL_Dehorsan 500 mg-200 mg-4 mg šumivý granulát_08.2025.pdf
Safety feature	No
Data update:	14.08.2023