NAUTISOL

This brand name is authorized in Cyprus, Hong Kong

Active ingredients

The drug NAUTISOL contains one active pharmaceutical ingredient (API):

1 Prochlorperazine
UNII 531SH87H9N - PROCHLORPERAZINE DIMETHANESULFONATE

Prochlorperazine belongs to the phenothiazine group. Prochlorperazine has a wide range of activity arising from its depressant actions on the CNS and its alpha-adrenergic blocking and weaker anti-muscarinic properties. It inhibits dopamine and prolactin-release-inhibitory factor, thus stimulating the release of prolactin.

Read about Prochlorperazine

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
NAUTISOL Tablet Υπουργείο Υγείας (CY) MPI, EU: SmPC

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC code Group title Classification
N05AB04 Prochlorperazine N Nervous system → N05 Psycholeptics → N05A Antipsychotics → N05AB Phenothiazines with piperazine structure
Discover more medicines within N05AB04

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
Country: HK Department of Health Drug Office Identifier(s): 25480, 35835

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