View the NEOSALINE registration information details.
Back to drug list
ItemsDrug Registration information
ID2861
No2861
Brand NameNEOSALINE
IngredientsSODIUM CHLORIDE BP 1.300G, POTASSIUM CHLORIDE BP 0.750G, SODIUM CITRATE BP 1.450G, ANHYDROUS GLUCOSE BP 6.750 G
Dosage FormPOWDER FOR ORAL SOLUTION
Primary PackagingSACHET
Storage
Shelf Life3 YEARS
Pack SizeBOX OF 50 SACHETS
Dispensing Category
ATC Classification
Pharmaceutical Class
IndicationsREPLACEMENT OF FLUID AND ELECTROLYTE LOSS DUE TO ACUTE DIARRHEA, VOMITING & DEHYDRATION, OTHER CONDITIONS OF FLUID LOSS OR LACK OF INTAKE IN PATIENTS OF ALL AGE GROUPS.
Contraindications
Side Effects
Unit Price
EDLNULL
DescriptionWHITE CRYSTALLINE, FREE FLOWING POWDER
Note
License OwnerVIMPEX (LAO) CO.,LTD
ManufacturerESKAYEF PHARMACEUTICALS LIMITED
CountryBANGLADESH
Import Registration No
Import Registration Date
ActivityCERTIFICATE RELEASED
Applied Date
FDD Registration No09 I 4584/18
FDD Registration Date07/07/2025
Expiry Date06/07/2030
Back to drug list
ADB ASEAN COVID-19 Laos JICA KOICA Global Fund WFP UHS Laos World Bank MOH Laos UNODC WHO SIDA