Registered Uganda · NDA

IRBESARTAN + HYDROCHLOROTHIAZIDE

NDA/MAL/HDP/11082 ORAL SOLID ORDINARY FILM-COATED TABLETS 150 MG + 12.5 MG

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Registration & product details

Registration no.
NDA/MAL/HDP/11082
Registration date
02/02/2024
Expiry date
-
Status
Registered
Active ingredient
-
Dosage form
ORAL SOLID ORDINARY FILM-COATED TABLETS
Strength
150 MG + 12.5 MG
Pack size
1.0X3.0X10.0 TABLET 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
United Pharmaceuticals Manufacturing Co UPM, Ubay Bin Muath St 57، عمّان، Jordan

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.