Registered Uganda · NDA

PARACETAMOL + DIPHENHYDRAMINE HYDROCHLORIDE

NDA/MAL/HDP/12147 ORAL SOLID ORDINARY FILM-COATED TABLETS 500 MG + 25 MG

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Registration & product details

Registration no.
NDA/MAL/HDP/12147
Registration date
05/01/2026
Expiry date
-
Status
Registered
Active ingredient
-
Dosage form
ORAL SOLID ORDINARY FILM-COATED TABLETS
Strength
500 MG + 25 MG
Pack size
1*2*10TABLET BLISTER
Therapeutic class
-
Manufacturer / MAH
Glaxosmithkline Dungarvan Limited, Dungarvan, Co. Waterford X35 Ry76
Applicant / LTR
GLAXOSMITHKLINE LIMITED
Country of origin
IRELAND
Manufacturer location
Lisfennel Cl, Knockbrack, Dungarvan, Co. Waterford, X35 Y983, Ireland

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.