View drug registration information details.
Items | Registration information |
ID | 353 |
No | 353 |
Brand Name | AMOXIN - CBF |
Ingredients | AMOXICILLIN SODIUM EQ. TO AMOXICILLIN 1G |
Dosage Form | POWDER FOR SOLUTION FOR INJECTION |
Primary Packaging | VIAL |
Storage | STORE IN A DRY PLACE, TEMPERATURE BELOW 25'C, PROTECTED FROM LIGHT. |
Shelf Life | 3 YEARS |
Pack Size | BOX OF 1VIAL AND 1 AMPOULE WITH 5ML WATER FOR INJECTION |
Dispensing Category | Prescription only |
ATC Classification | J01CA04 |
Pharmaceutical Class | ANTIBACTERIA |
Indications | UPPER RESPIRATORY TRACT INFECTIONS, OTITIS MEDIA, ACUTE AN DBRONCHIAL BRONCHITIS, CHRONIC BRONCHIAL SEPSIS, CYSTITIS, URETHRITIS, PYELONEPHRITIS, BACTERIURIA IN PREGNANCY, GYNAECOLOGICAL INFECTION, GONORRHEA, SEPTICAEMIA, TYPHOID AND PARATHYPHOID FEVER, SKIN AND SOFT TISSUE INFECTION… |
Contraindications | PENICILLIN HYPERSENSITIVITY .
GLANDULAR FEVER AND LYMPHATIC LYMPHOMA.
BACTERIAL RESISTANCE TO AMOXICILLIN OR AMPICILLIN. |
Side Effects | THE MOST COMMON ADVERSE EFFECTS ARE SENSITIVITY REACTIONS INCLUDING URTICARIA, MACULO-PAPULAR RASHES. |
Unit Price | - |
EDL |
Yes |
Description | WHITE OR ALMOST WHITE POWDER |
Note | |
License Owner | CBF PHARMA CO.,LTD |
Manufacturer | NORTH CHINA PHARMACEUTICAL CO., LTD |
Country | CHINA |
Import Registration No | GYZZH20023133 |
Import Registration Date | 2010-09-25 |
Activity | CERTIFICATE RELEASED |
Applied Date | 2022-03-21 |
FDD Registration No | 11 I 3925/13 |
FDD Registration Date | 2022-09-26 |
Expiry Date | 2025-09-25 |
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