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Registered Uganda · NDA

CEFTRIAXONE

NDA/MAL/HDP/2642 PARENTERAL ORDINARY DRY VIALS 1G

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Registration & product details

Registration no.
NDA/MAL/HDP/2642
Registration date
01/07/2016
Expiry date
-
Status
Registered
Active ingredient
-
Strength
1G
Pack size
1.0X1.0 G VIAL + 10 ML AMPOULE WFI
Therapeutic class
-
Manufacturer / MAH
Medochemie
Applicant / LTR
MEDOCHEMIE LTD
Country of origin
CYPRUS
Manufacturer location
Michael Irakleous 2 4101, Agios Athanasios 4101, Cyprus

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.