Registered Uganda · NDA

ARTESUNATE

NDA/MAL/HDP/2055 PARENTERAL ORDINARY DRY VIALS 120MG

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Registration & product details

Registration no.
NDA/MAL/HDP/2055
Registration date
01/07/2011
Expiry date
-
Status
Registered
Active ingredient
-
Dosage form
PARENTERAL ORDINARY DRY VIALS
Strength
120MG
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
Therapeutic class
-
Manufacturer / MAH
Guilin Pharmaceutical Co. Ltd
Applicant / LTR
GUILIN PHARMACEUTICAL CO. LTD.
Country of origin
CHINA
Manufacturer location
43 Qi Li Dian Lu, Qi Xing Qu, Gui Lin Shi, Guang Xi Zhuang Zu Zi Zhi Qu, China, 541010

Source: National Drug Authority · fetched 2026-04-21 17:37:06 · updated 2026-09-12 04:00:21

Disclaimer: This information is sourced from National Drug Authority (Uganda). Always consult a qualified healthcare professional before using any medication.