Registered Uganda · NDA

ARTESUNATE

NDA/MAL/HDP/8359 PARENTERAL ORDINARY DRY VIALS 120MG

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Registration & product details

Registration no.
NDA/MAL/HDP/8359
Registration date
29/11/2017
Expiry date
-
Status
Registered
Active ingredient
-
Dosage form
PARENTERAL ORDINARY DRY VIALS
Strength
120MG
Pack size
1.0X120.0 MG VIAL + 1*10 ML SODIUM CHLORIDE IN GLASS AMPOULE + 1*2 ML SODIUM BICARBONATE IN GLASS AMPOULE
Therapeutic class
-
Manufacturer / MAH
Indasi Lifescience Pvt. Ltd
Applicant / LTR
ABACUS PHARMA (A) LTD.
Country of origin
INDIA
Manufacturer location
FV56+WX8, Bhimpore, Daman, Dadra and Nagar Haveli and Daman and Diu 396210, India

Source: National Drug Authority · fetched 2026-04-21 17:37:09 · 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.