View drug registration information details.
| Items | Registration information |
|---|
| ID | 485 |
|---|
| No | 485 |
|---|
| Brand Name | FLONOXIN 400 MG TABLET |
|---|
| Ingredients | MOXIFLOXACIN HYDROCHLORIDE 436.34 MG EQ.TO MOXIFLOXACIN 400 MG |
|---|
| Dosage Form | FILM COATED TABLET |
|---|
| Primary Packaging | PVC-BLISTER |
|---|
| Storage | |
|---|
| Shelf Life | 2 YEARS |
|---|
| Pack Size | BOX OF 1 X 5'S AND 2 X 5'S |
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| Dispensing Category | |
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| ATC Classification | |
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| Pharmaceutical Class | |
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| Indications | ACUTE BACTERIAL RHINOSINUSITIS, ACUTE EXACERBATIONS OF CHRONIC OBSTRUCTIVE PULMONARY DISEASE INCLUDING CHRONIC BRONCHITIS, NOSOCOMIAL PNEUMONIA/HOSPITAL-ACQUIRED PNEUMONIA, ACUTE OTITIS MEDIA, EXTERNAL OTITIS, ENDOCARDITIS, MENINGITIS, SEPTICAEMIA, COMPLICATED SKIN AND SKIN SREUCTURE INFECTION |
|---|
| Contraindications | |
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| Side Effects | |
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| Unit Price | |
|---|
| EDL |
NULL |
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| Description | DULL RED, 17 MM OBLONG SHAPED, PLAIN ON BOTH SIDES, FILM COATED TABLET |
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| Note | |
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| License Owner | DKSH LAOS COMPANY LIMITED |
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| Manufacturer | DUOPHARMA MANUFACTURING(BANGI)SDN.BHD. |
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| Country | MALAYSIA |
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| Import Registration No | |
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| Import Registration Date | |
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| Activity | CERTIFICATE RELEASED |
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| Applied Date | |
|---|
| FDD Registration No | 04 I 5466/23 |
|---|
| FDD Registration Date | 11-APR-2023 |
|---|
| Expiry Date | 10-APR-2026 |
|---|
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