Regulatory PathRegulatory requirements compared

Active substance

Piracetam

Open in the medicines table

SFDA Saudi Arabia — SFDA human drug list

Trade nameStrengthForm · routePackPublic priceTypeCompanyStatus
NOOTROPIL 12GM-60ML INFUSION SOLU20 mg/mlSolution for injection · Intravenous use1 VialSAR 25.85NCE · PrescriptionGLAXOSMITHKLINE (GSK)Withdrawn by MAH · Not Marketed
NOOTROPIL 800 MG FILM COATED800 mgFilm-coated tablet · Oral use30 BlisterSAR 27.95NCE · PrescriptionGlaxo Saudi Arabia Ltd.Withdrawn by MAH · Not Marketed
NOOTROPIL AMP 1GM-5ML200 mg/mlSolution for injection · Intravenous use12 AmpouleSAR 29.25NCE · PrescriptionGLAXOSMITHKLINE (GSK)Withdrawn by MAH · Not Marketed
NOOTROPIL AMP 1GM-5ML200 mg/mlSolution for injection · Intravenous use4 AmpouleSAR 23.10NCE · PrescriptionGLAXOSMITHKLINE (GSK)Withdrawn by MAH · Not Marketed
NOOTROPIL CAPS 400MG400 mgCapsule · Oral use60 BlisterSAR 28.90NCE · PrescriptionGLAXOSMITHKLINE (GSK)Withdrawn by MAH · Not Marketed
NOOTROPIL SOLN 20%200 mg/mlOral solution · Oral use1 BottleSAR 32.65NCE · PrescriptionGLAXOSMITHKLINE (GSK)Withdrawn by MAH · Not Marketed
PIRACETAM CAPS 400MG400 mgCapsule, hard · Oral use20 BlisterSAR 8.95Generic · PrescriptionALMIRALL PRODES PHARMA S.A.Withdrawn by MAH · Not Marketed

Prices — United States and England

SourceProduct as listedPriceUnit / packDate
NHS Drug TariffPiracetam 1.2g tablets£10.9760 tablet1 Oct 2026
NHS Drug TariffPiracetam 800mg tablets£11.7590 tablet1 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.

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.