Registered Uganda · NDA

NEBIVOLOL HYDROCHLORIDE + HYDROCHLOROTHIAZIDE

NDA/MAL/HDP/6625 ORAL SOLID ORDINARY FILM-COATED TABLETS 5MG + 12.5MG

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Registration & product details

Registration no.
NDA/MAL/HDP/6625
Registration date
01/07/2016
Expiry date
-
Status
Registered
Active ingredient
-
Strength
5MG + 12.5MG
Pack size
1.0X2.0X14.0 TABLET BLISTER,1.0X1.0X4.0 TABLET BLISTER (FREE MEDICAL SAMPLE)
Therapeutic class
-
Country of origin
GERMANY
Manufacturer location
Tempelhofer Weg 83, 12347 Berlin, Germany

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.