View drug registration information details.

Items	Registration information
ID	46
No	46
Brand Name	FLOCTIL 250
Ingredients	AZITHROMYCIN DIHYDRATE EQ. TO AZITHROMYCIN 250 MG
Dosage Form	CAPSULE
Primary Packaging	ALU-PVC/PVDC
Storage	STORE AT TEMPERATURE NOT MORE THAN 30"C
Shelf Life	3 YEARS
Pack Size	BOX OF 10 X 6'S
Dispensing Category	PRESCRIPTION ONLY
ATC Classification	J01FA10
Pharmaceutical Class	ANTIBACTERIA
Indications	AZITHROMYCIN IS INDICATED FOR THE TREATMENT OF BRONCHITIS, COMMUNITY - ACQUIRED PNEUMONIA, SINUSITIS, PHARYNGITIS/ TONISILITIS, OTITIS, MEDIA, SKIN AND SOFT TISSUE INFECTIONS AND UNCOMPLICATED GENITAL INFECTIONS DUE TO CHLAMYDIA TRACHOMATIS, CONSIDERATIONS SHOULD BE GIVEN TO OFFICIAL GUIDANCE REGARDING THE APPROPRIATE USE OF ANTIBACTERIAL AGENTS
Contraindications	AZITHROMYCIN IS CONTRAINDICATED IN PATIENTS WITH A KNOWN HYPERSENSITIVITY TO THE ACTIVE SUBSTANCE OR ANY MACROLIDES ANTIBIOTICS. BECAUSE OF THE THEORETICAL POSSIBILITY OF ERGOTISM, FLOCTIL 250 AND ERGOT DERIVATIVE SHOULD NOT BE CO-ADMINISTERED
Side Effects	HEPATOBILIARY DISORDERS : HEPATITIS AND CHOLESTATIC JAUNDICE HAVE BEEN REPORTED, AS WELL AS RARE CASES OF HEPATIC, GI DISORDERS(NAUSEA, VOMITING, DIARRHEA, ABDOMINAL DISCOMFORT)
Unit Price	-
EDL	Yes
Description	WHITE POWDER IN OPAQUE WHITE /WHITE CAPSULE NO. 0 WITH PRINTED 250 AND AZ IN BLACK COLOR
Note
License Owner	AI KEN PHARMA CO., LTD
Manufacturer	UNISON LABORATORIES CO., LTD
Country	THAILAND
Import Registration No	1A 47/50 ( NG)
Import Registration Date	27/08/2007
Activity	CERTIFICATE RELEASED
Applied Date	2022-09-28
FDD Registration No	05 I 4153/16
FDD Registration Date	2023-02-02
Expiry Date	2026-02-01

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