View the LOSART PLUS registration information details.
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ItemsDrug Registration information
ID2078
No2078
Brand NameLOSART PLUS
IngredientsLOSARTAN POTASSIUM USP 50 MG HYDROCHLOROTHIAZIDE BP 12.5 MG
Dosage FormFILM-COATED TABLETS
Primary PackagingALU-ALU BLISTER
Storage
Shelf Life2 YEARS
Pack SizeBOX OF 3 X 10'S
Dispensing Category
ATC Classification
Pharmaceutical Class
Indications FOR THE TREATMENT OF HYPERTENSION, FOR PATIENTS IN WHOM COMBINATION THERAPY IS APPROPRIATE.
Contraindications
Side Effects
Unit Price
EDLNULL
DescriptionYELLOW, TRIANGULAR , BICONVEX FILM COATED TABLET ENGRAVED WITH "ACME" WITH ONE FACE AND A BREAK LINE ON THE OTHER FACE.
Note
License OwnerPALAMY PHARMA CO., LTD
ManufacturerTHE ACME LABORATORIES LTD.
CountryBANGLADESH
Import Registration No
Import Registration Date
ActivityCERTIFICATE RELEASED
Applied Date
FDD Registration No03 I 3734/12
FDD Registration Date31/03/2023
Expiry Date30/03/2026
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