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Medicines & clinical reference

Uganda register

Generic formulationARTESUNATE

Strength: 120MG
Dosage form: PARENTERAL ORDINARY DRY VIALS
Pack size: 1.0X120.0 MG VIAL + 1 *2 ML AMPOULE OF 5% SODIUM BICARBONATE SOLUTION + 1*10 ML AMPOULE OF 0.9% SODIUM CHLORIDE

Jurisdiction: UGSource: July 2024 register

No clinical monograph is available for this medicine.

This record currently contains product and registration details. No clinical monograph is available for this medicine.

Product record and document traceability

Registration number: NDA/MAL/HDP/2055
Jurisdiction: Uganda (UG)
License holder: SHANGHAI FOSUN PHARMACEUTICAL DEVELOPMENT CO. LTD
Local representative: TRIDEM PHARMA UGANDA LIMITED
Manufacturing site: GUILIN PHARMACEUTICAL CO. LTD.NO. 43 QILIDIAN ROAD, GUILIN 541004
Country of manufacture: CHINA
Registration date: 01/07/2011
Source: Uganda National Drug Register, July 2024 · Page 862