Registered Uganda · NDA

LOSARTAN POTASSIUM + HYDROCHLOROTHIAZIDE

NDA/MAL/HDP/9901 ORAL SOLID ORDINARY FILM-COATED TABLETS 50MG + 12.5MG

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Registration & product details

Registration no.
NDA/MAL/HDP/9901
Registration date
11/12/2021
Expiry date
-
Status
Registered
Active ingredient
-
Strength
50MG + 12.5MG
Pack size
1*1*10TABLET BLISTER
Therapeutic class
-
Applicant / LTR
ROYAL PHARMA 2011 LIMITED
Country of origin
INDIA
Manufacturer location
B-21/22, MIDC Area, Kalmeshwar, Nagpur, Kalmeshwar-Bramhni, Maharashtra 441501, India

Source: National Drug Authority · fetched 2026-05-12 08:00:47 · 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.