Registered Uganda · NDA

ANHYDROUS GLUCOSE+SODIUM CHLORIDE+TRISODIUM CITRATE+POTASSIUM CHLORIDE/ZINC,ANHYDROUS GLUCOSE+SODIUM CHLORIDE+TRISODIUM CITRATE+POTASSIUM CHLORIDE/ZINC,ANHYDROUS GLUCOSE+SODIUM CHLORIDE+TRISODIUM CITRATE+POTASSIUM CHLORIDE/ZINC

NDA/MAL/HDP/0088 ORAL LIQUID ORDINARY COMBINATION PACK POWDERS/GRANULES 2.7MG+0.52MG+0.58MG+0.30MG+20MG PER 200ML,6.75MG+1.30MG+1.45MG+0.75MG+20MG PER 500ML SACHET,13.5MG+2.60MG+2.90MG+1.50MG+20MG PER 1000ML SACHET

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Registration & product details

Registration no.
NDA/MAL/HDP/0088
Registration date
01/07/2015
Expiry date
-
Status
Registered
Active ingredient
-
Strength
2.7MG+0.52MG+0.58MG+0.30MG+20MG PER 200ML,6.75MG+1.30MG+1.45MG+0.75MG+20MG PER 500ML SACHET,13.5MG+2.60MG+2.90MG+1.50MG+20MG PER 1000ML SACHET
Pack size
4.0X500.0 ML SACHET + 1*10 BLISTERS,10.0X200.0 ML SACHET + 1*10 BLISTERS,2.0X1000.0 ML SACHET + 1*10 BLISTERS
Therapeutic class
-
Manufacturer / MAH
Agog Pharma Ltd
Country of origin
INDIA
Manufacturer location
33, Gaonraipada Sector 2,The Taluka Ind. co. op. estate, Vasai, Bilalpada, Golani Naka, Vasai East, Vasai-Virar, Maharashtra 401208, India

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.