Registered Uganda · NDA

MOXIFLOXACIN HYDROCHLORIDE

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Registration & product details

Registration no.
NDA/MAL/HDP/6457
Registration date
01/07/2017
Expiry date
-
Status
Registered
Active ingredient
-
Strength
400MG
Pack size
I. 1*2*5TABLET BLISTER
Therapeutic class
-
Manufacturer / MAH
Aurobindo Pharma Limited
Applicant / LTR
AUROBINDO PHARMA LIMITED
Country of origin
INDIA
Manufacturer location
R4HP+9VG, Raipalle, Telangana 509202, India

Source: National Drug Authority · fetched 2026-04-21 17:37:08 · 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.