Registered Uganda · NDA

HYDROCHLOROTHIAZIDE + IRBESARTAN

NDA/MAL/HDP/10193 ORAL SOLID ORDINARY FILM-COATED TABLETS 12.5 MG + 300 MG

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Registration & product details

Registration no.
NDA/MAL/HDP/10193
Registration date
09/09/2022
Expiry date
-
Status
Registered
Active ingredient
-
Dosage form
ORAL SOLID ORDINARY FILM-COATED TABLETS
Strength
12.5 MG + 300 MG
Pack size
I. 1*3*10TABLET BLISTER
Therapeutic class
-
Manufacturer / MAH
United Pharmaceuticals Manufacturing Limited Company Al-rageem, Sahab, P.o. Box
Applicant / LTR
UNITED PHARMACEUTICALS MANUFACTURING LIMITED COMPANY
Country of origin
JORDAN
Manufacturer location
Jordan Insurance Co JIC Complex، Prince Muhammad St 257, Amman, Jordan

Source: National Drug Authority · fetched 2026-04-21 17:37:05 · updated 2026-09-12 04:00:19

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