Registered Uganda · NDA

IBUPROFEN+PARACETAMOL

NDA/MAL/HDP/1067 ORAL LIQUID ORDINARY SUSPENSIONS 200MG+ 250MG/10ML

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Registration & product details

Registration no.
NDA/MAL/HDP/1067
Registration date
01/07/2010
Expiry date
-
Status
Registered
Active ingredient
-
Strength
200MG+ 250MG/10ML
Pack size
1.0X100.0 ML BOTTLE
Therapeutic class
-
Country of origin
INDIA
Manufacturer location
C-83, Phase 7, Industrial Area, Sector 74, Sahibzada Ajit Singh Nagar, Punjab 160055, India

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.