| ID | 488 |
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| No | 488 |
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| Brand Name | DILANTIN (INFATAB) |
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| Ingredients | PHENYTOIN 50 MG |
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| Dosage Form | TABLET |
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| Primary Packaging | BOTTLE |
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| Storage | STORE BELOW 30'C |
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| Shelf Life | 60 MONTHS |
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| Pack Size | 250 TABLETS PER BOTTLE |
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| Dispensing Category | Prescription only |
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| ATC Classification | N03AB02 |
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| Pharmaceutical Class | ANTISEIZURE |
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| Indications | PHENYTOIN IS INDICATED FOR THE CONTROL OF GENERALIZED TONIC-CLONIC ( GRAND MAL) AND COMPLEX PARTIAL (PSYCHOMOTOR, TEMPORAL LOBE) SEIZURES AND PREVENTION AND TREATMENT OF SEIZURES OCCURRING DURING OR FOLLOWING NEUROSURGERY. |
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| Contraindications | PHENYTOIN IS CONTRAINDICATED IN THOSE PATIENTS WHO ARE HYPERSENSITIVE TO PHENYTOIN |
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| Side Effects | * BODY AS A WHOLE : ANAPHYLACTOID REACTION, AND ANAPHYLAXIS. |
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| Unit Price | USD 4.27/ |
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| EDL |
Yes |
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| Description | YELLOW, TRIANGULAR TABLET HAVING FLAT SIDE, BEVELED EDGES, A BREAKING LINE ON ONE SIDE AND THE PARCODE '' VLE 007'' ON THE OTHER SIDE. |
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| Note | |
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| License Owner | DKSH LAOS COMPANY LIMITED |
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| Manufacturer | OLIC (THAILAND) LIMITED |
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| Country | THAILAND |
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| Import Registration No | 1A 36/40 |
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| Import Registration Date | 1997-01-09 |
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| Activity | CERTIFICATE RELEASED |
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| Applied Date | 02-ส.ค.-2024 |
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| FDD Registration No | 11 I 3996/13 |
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| FDD Registration Date | 2024-09-25 |
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| Expiry Date | 2029-09-24 |
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