Registered Uganda · NDA

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

NDA/MAL/HDP/6190 ORAL LIQUID ORDINARY SOLUBLE POWDERS 2.7MG+0.52MG+0.58MG+0.30MG PER 200ML SACHET,6.75MG+1.30MG+1.45MG+0.75MG PER 500ML SACHET,13.5MG+2.60MG+2.90MG+1.50MG PER 1000ML SACHET

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Registration & product details

Registration no.

NDA/MAL/HDP/6190

Registration date

01/07/2015

Expiry date

Status

Registered

Active ingredient

Dosage form

ORAL LIQUID ORDINARY SOLUBLE POWDERS

Strength

2.7MG+0.52MG+0.58MG+0.30MG PER 200ML SACHET,6.75MG+1.30MG+1.45MG+0.75MG PER 500ML SACHET,13.5MG+2.60MG+2.90MG+1.50MG PER 1000ML SACHET

Pack size

1.0X500.0 ML SACHET,1.0X1000.0 ML SACHET,1.0X200.0 ML SACHET

Therapeutic class

Manufacturer / MAH

Agog Pharma Ltd

Applicant / LTR

GITTOES PHARMACEUTICALS LIMITED

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 17:37:08 · 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.