| ID | 630 |
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| No | 630 |
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| Brand Name | VIGAMOX |
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| Ingredients | MOXIFLOXACIN HYDROCHLORIDE 5.45 MG EQ.TO MOXIFLOXACIN BASE 5 MG |
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| Dosage Form | OPHTHALMIC SOLUTION |
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| Primary Packaging | BOTTLE |
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| Storage | DO NOT STORE ABOVE 25. C |
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| Shelf Life | 3 YEARS |
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| Pack Size | 5 ML/BOTTLE/BOX |
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| Dispensing Category | Prescription only |
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| ATC Classification | XX |
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| Pharmaceutical Class | ANTI-INFECTIVES |
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| Indications | TREATMENT OF BACTERIAL CONJUNCTIVITIS CAUSED BY SUSCEPTIBLE STRAINS OF GRAM-POSITIVE AND GRAM-NEGATIVE BACTERIA. |
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| Contraindications | VIAGMOX SOLUTION IS CONTRAINDICATED IN PATIENTS WITH A HISTORY OF HYPERSENSITIVITY TO MOXIFLOXACINE,TO OTHER QUINOLONES , OR TO ANY OF THE COMPONENTS IN THIS MEDICATION |
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| Side Effects | NO SERIOUS OPHTHALMIC OR SYSTEMIC ADVERSE REACTIONS RELATED TO VIGAMOX SOLUTION WERE REPORTED. ADVERSE REACTIONS WERE GENERALLY MILD AND OCCURRED AT AN INCIDENCE SIMILAR TO PLACEBO (VEHICLE) THE MOST FREQUENTLY REPORTED EVENT WAS TRANSIENT OCULAR PAIN, DI |
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| Unit Price | - |
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| EDL |
No |
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| Description | CLEAR, GREENISH YELLOW SOLUTION, ESSENTIALLY PARTICLE FREE |
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| Note | |
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| License Owner | DKSH LAOS COMPANY LIMITED |
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| Manufacturer | ALCON - COUVREUR NV |
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| Country | BELGIUM |
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| Import Registration No | BE350707 |
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| Import Registration Date | 2009-10-22 |
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| Activity | CERTIFICATE RELEASED |
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| Applied Date | 2022-01-27 |
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| FDD Registration No | 04 I 5487/23 |
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| FDD Registration Date | 2023-04-25 |
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| Expiry Date | 2026-04-24 |
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