Regulatory PathRegulatory requirements compared

Active substance

Fat emulsions

Open in the medicines table

SFDA Saudi Arabia — SFDA human drug list

Trade nameStrengthForm · routePackPublic priceTypeCompanyStatus
INTRALIPID 10% (SOYBEAN OIL)10 %Infusion · Parenteral use1 BottleSAR 67.60Generic · PrescriptionOCTAPHARMAWithdrawn by MAH · Not Marketed
INTRALIPID 10% (SOYBEAN OIL)10 %Infusion · Parenteral use1 BottleSAR 15.40Generic · PrescriptionOCTAPHARMAWithdrawn by MAH · Not Marketed
INTRALIPID 20% (SOYBEAN OIL)20 %Infusion · Parenteral use1 BottleSAR 104.75Generic · PrescriptionOCTAPHARMAWithdrawn by MAH · Not Marketed
INTRALIPID 20% (SOYBEAN OIL)20 %Infusion · Parenteral use1 BottleSAR 35.65Generic · PrescriptionOCTAPHARMAWithdrawn by MAH · Not Marketed
LIPOSYN 10% (SAFFLOWER OIL)10 %Infusion · Parenteral use1 BottleSAR 13.10Generic · PrescriptionHOSPIRA INCWithdrawn by MAH · Not Marketed
LIPOSYN II 20% (SOYABEEN OIL)20 %Solution · Parenteral use1 BottleSAR 94.85Generic · PrescriptionHOSPIRA INCWithdrawn by MAH · Not Marketed
LIPOSYN II 20% (SOYABEEN OIL)20 %Infusion · Parenteral use1 BottleSAR 45.55Generic · PrescriptionHOSPIRA INCWithdrawn by MAH · Not Marketed
LIPOSYN II 20% (SOYABEEN OIL)20 %Infusion · Parenteral use1 BottleSAR 45.55Generic · PrescriptionAbbott LaboratoriesInvalid · Not Marketed
LIPOVENOS 10% (SOYBEAN OIL)10 %Infusion · Parenteral use1 BottleSAR 60.00Generic · PrescriptionFRESENIUS KABIWithdrawn by MAH · Not Marketed
LIPOVENOS 20% (SOYBEAN OIL)20 %Infusion · Parenteral use1 BottleSAR 64.60Generic · PrescriptionFRESENIUS KABIWithdrawn by MAH · Not Marketed

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.