Registered Uganda · NDA

MOXIFLOXACIN HYDROCHLORIDE

NDA/MAL/HDP/10998 PARENTERAL ORDINARY INFUSION VIALS/BOTTLES 400MG/100ML

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Registration & product details

Registration no.
NDA/MAL/HDP/10998
Registration date
17/08/2023
Expiry date
-
Status
Registered
Active ingredient
-
Dosage form
PARENTERAL ORDINARY INFUSION VIALS/BOTTLES
Strength
400MG/100ML
Pack size
1.0X1.0X100.0 ML BOTTLE
Therapeutic class
-
Manufacturer / MAH
Abacus Parenteral Drugs Limited
Applicant / LTR
ABACUS PARENTERAL DRUGS LIMITED
Country of origin
UGANDA
Manufacturer location
Jinja Kampala Road, Mukono, Uganda

Source: National Drug Authority · fetched 2026-04-21 17:37:05 · updated 2026-09-12 04:00:20

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