Registered Uganda · NDA

MOXIFLOXACIN HYDROCHLORIDE

NDA/MAL/HDP/11065 OPHTHALMIC DROPS 0.5 %W/V

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Registration & product details

Registration no.
NDA/MAL/HDP/11065
Registration date
13/12/2023
Expiry date
-
Status
Registered
Active ingredient
-
Dosage form
OPHTHALMIC DROPS
Strength
0.5 %W/V
Pack size
I. 1*1*5ML BOTTLE
Therapeutic class
-
Country of origin
SAUDI ARABIA
Manufacturer location
Jeddah 1st Industrial City, Jeddah 21442, Saudi Arabia

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.