View the ZYLTAN H registration information details.
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ItemsDrug Registration information
ID614
No614
Brand NameZYLTAN H
IngredientsLOSARTAN POTASSIUM USP 50 MG, HYDROCHLOROTHIAZIDE USP 12.5 MG
Dosage FormFILM COATED TABLET
Primary PackagingALU-ALU BLISTER
Storage
Shelf Life2 YEARS
Pack SizeBOX OF 3 X 10 TABLETS
Dispensing Category
ATC Classification
Pharmaceutical Class
IndicationsTREATMENT OF HYPERTENSION IN PATIENTS REQUIRING BOTH LOSARTAN AND HYDROCHLOROTHIAZIDE.
Contraindications
Side Effects
Unit Price
EDLNULL
DescriptionREDDISH BROWN COLORED, OBLONG SHAPED, FILM COATED TABLET HAVING A BREAK LINE ON ONE SIDE
Note
License OwnerDKSH LAOS COMPANY LIMITED
ManufacturerTROIKAA PHARMACEUTICALS LIMITED
CountryINDIA
Import Registration No
Import Registration Date
ActivityCERTIFICATE RELEASED
Applied Date
FDD Registration No05 I 5102/21
FDD Registration Date08/04/2024
Expiry Date07/04/2027
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