View the LANZAAR 50 registration information details.
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ItemsDrug Registration information
ID209
No209
Brand NameLANZAAR 50
IngredientsLOSARTAN POTASSIUM 50 MG
Dosage FormFILM-COATED TABLETS
Primary PackagingALU-PVDC BLISTERPACK
Storage
Shelf Life2 YEARS AFTER MANUFACTURE
Pack Size3 X 10'S /BOX
Dispensing Category
ATC Classification
Pharmaceutical Class
IndicationsTREATMENT OF HYPERTENSION (HTN), DIABETIC NEPHROPATHY IN PATIENTS WITH TYPE 2 DIABETES MELLITUS( NIDDM) AND A HISTORY OF HYPERTENSION. STROKE RISK REDUCTION IN PATIENTS WITH HTN AND LEFT VENTRICULAR HYPERTROPHY
Contraindications
Side Effects
Unit Price
EDLNULL
DescriptionWHITE OVAL BICONVEX FILM COATED TABLETS WITH ''BERLIN'' ON ONE SIDE AND SCORED BETWEEN "L" AND "50" ON THE OTHER SIDE
Note
License OwnerBERLIN PHARMA LAO CO.,LTD
ManufacturerBERLIN PHARMACEUTICAL INDUSTRY CO., LTD.
CountryTHAILAND
Import Registration No
Import Registration Date
ActivitySTEP 1: RECEIVE (RENEW)
Applied Date27/06/2025
FDD Registration No03 I 3710/12
FDD Registration Date14/09/2022
Expiry Date13/09/2025
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