Safety Alert

Important identified signals on Artemether Lumefantrine (Alert)

Registered Uganda · NDA

ARTEMETHER

NDA/MAL/HDP/3591 PARENTERAL ORDINARY I M AMPOULES 80MG/ML

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Registration & product details

Registration no.
NDA/MAL/HDP/3591
Registration date
01/07/1998
Expiry date
-
Status
Registered
Active ingredient
-
Dosage form
PARENTERAL ORDINARY I M AMPOULES
Strength
80MG/ML
Pack size
1.0X5.0X1.0 ML AMPOULE
Therapeutic class
-
Manufacturer / MAH
Anfarm Hellas S.a
Applicant / LTR
DAFRA PHARMA LTD
Country of origin
GREECE |
Manufacturer location
Athinon - Lamias National Rd (61th km, Schimatari 320 09, Greece

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.