Regulatory PathRegulatory requirements compared

Active substance

Procyclidine

Open in the medicines table

SFDA Saudi Arabia — SFDA human drug list

Trade nameStrengthForm · routePackPublic priceTypeCompanyStatus
KEMADRIN 5MG TABLET5 mgTablet · Oral use100 Tablet ContainerSAR 26.95Generic · PrescriptionASPEN PHARMA TRADING LIMITED (APTL)Valid
KEMADRIN 5MG TABLET5 mgTablet · Oral use100 Tablet ContainerSAR 27.00Generic · PrescriptionASPENWithdrawn by MAH · Not Marketed
KEMADRIN INJ 10MG-2ML5 mg/mlSolution · Intravenous use5 AmpouleSAR 30.10NCE · PrescriptionGLAXOWELLCOMEWithdrawn by MAH · Not Marketed
KEMADRIN TABS 5 MG5 mgTablet · Oral use100 BlisterSAR 27.30NCE · PrescriptionGLAXOWELLCOMEWithdrawn by regulatory authority · Not Marketed
Indications — CHI Daman Drug Formulary

PARKINSONISM; SCHIZOPHRENIA

US FDA United States — FDA approvals (Drugs@FDA)

ProductStrengthForm · routeApplicantStatusFirst approved
KEMADRIN5MG; 2MGtablet · oralMONARCH PHARMSDiscontinued27 Jul 1955

Prices — United States and England

SourceProduct as listedPriceUnit / packDate
NHS Drug TariffProcyclidine 10mg/2ml solution for injection ampoules£72.505 ampoule1 Oct 2026
NHS Drug TariffProcyclidine 2.5mg/5ml oral solution sugar free£51.17150 ml1 Oct 2026
NHS Drug TariffProcyclidine 5mg tablets£1.3028 tablet1 Oct 2026
NHS Drug TariffProcyclidine 5mg/5ml oral solution sugar free£75.78150 ml1 Oct 2026

NADAC: average price US retail pharmacies pay to buy the medicine. NHS Drug Tariff Part VIIIA: basic price reimbursed to pharmacies in England and Wales.

Safety signals and safety-related labeling changes

All safety entries for procyclidine →

Values as published by each source: SFDA human drug list (4-2026, as published by the Council of Health Insurance; indications from the CHI Daman Drug Formulary), Drugs@FDA, EMA medicines data, Health Canada Drug Product Database (Open Government Licence – Canada), CMS NADAC, NHS Drug Tariff Part VIIIA (NHSBSA Copyright, Open Government Licence v3.0), WHO Model List of Essential Medicines (CC BY 3.0 IGO; regrouped by active substance, not created by WHO), EMA PRAC, US FDA safety-related labeling changes and MHRA Drug Safety Update (Open Government Licence v3.0). Sources and reuse. Not a substitute for the official registers or the product information.