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ItemsRegistration information
ID266
No266
Brand NameAMOXICAP 500
IngredientsAMOXYCILLIN TRIHYDRATE EQ.TO AMOXYCILLIN 500 MG
Dosage FormCAPSULE
Primary PackagingBLISTERPACK
StorageSTORE BELOW 30 C, PROTECT FROM LIGHT
Shelf Life3 YEARS
Pack SizeBOX OF 10 X 10'S
Dispensing CategoryPrescription only
ATC ClassificationJ01CA04
Pharmaceutical ClassANTIBACTERIA
IndicationsEAR, NOSE AND THROAT INFECTIONS CAUSED BY STREPTOCOCCI, PNEUMOCOCCI, NON-PENICILLINASE-PRODUCING STAPHYLOCOCCI AND H.INFLUENZA, GENITOURINARY TRACT INFECTION CAUSED BY E.COLI, P.MIRABILIS, S.FAECALIS, SKIN AND SOFT TISSUE INFECTION CAUSED BY STREPTOCOCCI, NON-PENICILLINASE-PRODUCING STAPHYLOCOCCI AND E.COLI, ANOGENITAL AND URETHRAL GONORRHOEA CAUSED BY N.GONORRHOEA
ContraindicationsPATIENTS KNOWN TO BE SENSITIVE PENICILLIN, AVOID IN PATIENTS WITH INFECTIOUS MONONUCLEOSIS BECAUSE OF INCREASED RISK OF SKIN RASHES
Side EffectsRASH, HEMOLYTIC ANEMIA, ANEMIA, DIARRHEA, NAUSEA, VOMITING, BLACK HAIRY TONGUE, GLOSSITIS, STOMATITIS, SORE MOUTH OR TONGUE, ACUTE INTERSTITIAL NEPHRITIS
Unit Price5.33
EDL Yes
DescriptionSCARLET OPAQUE/YELLOW OPAQUE CAPSULE WITH AX500 PRINTED ON ONE END AND HD PRINTED ON THE OTHER END CAPSULE SIZE: 0, FILL MATERIAL: OFF-WHITE POWDER
Note
License OwnerBMS PHARMA SOLE CO.,LTD
ManufacturerHOVID BHD
CountryMALAYSIA
Import Registration NoMAL19950253AZ
Import Registration Date2016-04-07
ActivityCERTIFICATE RELEASED
Applied Date2022-03-29
FDD Registration No04 I 4685/19
FDD Registration Date2022-09-08
Expiry Date2025-09-07

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