View the AMOXICLAV registration information details.
Back to drug list
ItemsDrug Registration information
ID1953
No1953
Brand NameAMOXICLAV
IngredientsAMOXICILLIN SODIUM EQ.TO AMOXICILLIN 1 G, CLAVULANATE POTASSIUM EQ.TO CLAVULANIC ACID 200 MG
Dosage FormPOWDER FOR INJECTION
Primary PackagingVIALS
Storage
Shelf Life3 YEARS
Pack SizeBOX OF 10 VIALS
Dispensing Category
ATC Classification
Pharmaceutical Class
IndicationsUPPER AND LOWER RESPIRATORY TRACT INFECTION, GENITOURINARY TRACT INFECTION, SKIN AND SOFT TISSUE INFECTION, BONE AND JOINT INFECTION,
Contraindications
Side Effects
Unit Price
EDLNULL
DescriptionWHITE OR ALMOST WHITE POWDER
Note
License OwnerNAKORNLUANG PHARMA EXPORT-IMPORT CO.,LTD
ManufacturerREYOUNG PHARMACEUTICAL CO.,LTD
CountryCHINA
Import Registration No
Import Registration Date
ActivityCERTIFICATE RELEASED
Applied Date
FDD Registration No01 I 5871/25
FDD Registration Date31/01/2025
Expiry Date30/01/2030
Back to drug list
ADB ASEAN COVID-19 Laos JICA KOICA Global Fund WFP UHS Laos World Bank MOH Laos UNODC WHO SIDA