STEMETIL

This brand name is authorized in Australia, Cyprus, Estonia, Finland, Hong Kong, Ireland, Malta, New Zealand, Singapore, United Kingdom

Active ingredients

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

1 Prochlorperazine
UNII I1T8O1JTL6 - PROCHLORPERAZINE MALEATE

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  
STEMETIL Solution for injection Medicines & Healthcare Products Regulatory Agency (GB) MPI, EU: SmPC
STEMETIL Tablet Medicines & Healthcare Products Regulatory Agency (GB) 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: AU Pharmaceutical Benefits Scheme Identifier(s): 2369Q, 2893G, 3477B, 5205Y, 5206B
Country: EE Ravimiamet Identifier(s): 1615025
Country: FI Lรครคkealan turvallisuus- ja kehittรคmiskeskus Identifier(s): 160523
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 144022, 14541, 162500, 181502, 23063, 27606
Country: HK Department of Health Drug Office Identifier(s): 31117
Country: IE Health Products Regulatory Authority Identifier(s): 47090, 61123, 61131, 61875
Country: MT Medicines Authority Identifier(s): AA770/05302
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 1991
Country: SG Health Sciences Authority Identifier(s): 01382P

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