View drug registration information details.

Items	Registration information
ID	540
No	540
Brand Name	LODOZ 2.5 MG/ 6.25 MG
Ingredients	BISOPROLOL FUMARATE 2.50 MG, HYDROCHLOROTHIAZIDE 6.25 MG
Dosage Form	FILM COATED TABLET
Primary Packaging	ALU-ALU BLISTER
Storage	DO NOT STORE ABOVE 30 C
Shelf Life	2 YEARS
Pack Size	BOX OF 30 TABLETS
Dispensing Category	Prescription only
ATC Classification	C07BB07
Pharmaceutical Class	ANTIHYPERTENSIVE
Indications	MILD TO MODERATE ESSENTIAL HYPERTENSION
Contraindications	ACUTE HEART FAILURE OR DURING EPISODES OF HEART FAILURE DECOMPENSATION REQUIRING I.V INOTROPIC THERAPY, CARDIOGENIC SHOCK, SECOND OR THIRD DEGREE AV BLOCK, SICK SINUS SYNDROME. SINOATRIAL BLOCK ,SYMPTOMATIC BRADUCARDIA AND HYPOTENSION, SEVERE BRONCHIAL ASTHMA
Side Effects	LOSS OF APPETITE, HYPERGLYCAEMIA, HYPERURICAEMIA, DEPRESSION, SLEEP DISORDER, DIZZINESS, HEADACHE, FEELING OF COLDNESS OR NUMBNESS IN EXTREMITIES, NAUSEA, VOMOTTING, DIARRHEA, CONSTIPATION, FATIGUE
Unit Price
EDL	Yes
Description	YELLOW, ROUND, BICONVEX UPPER SIDE EMBOSSED HEART, DOWNSIDE EMBOSSED 2.5
Note
License Owner	DKSH LAOS COMPANY LIMITED
Manufacturer	MERCK HEALTHCARE KGaA
Country	FRANCE
Import Registration No	386 963-2 OR 34009 386 9636 2 5
Import Registration Date	2001-10-07
Activity	CERTIFICATE RELEASED
Applied Date	2024-02-14
FDD Registration No	12 I 5012/20
FDD Registration Date	2024-04-08
Expiry Date	2027-04-07

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