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Warning Date
    2017-10-03

SFDA Withdrawal a Batch for the Profinal Susp 100mg-5ml (110ml) which Produced by the manufacturer JULPHAR duo to Quality Defect

2017-10-03


SFDA is alerting all health facilities on circulation to stop using the above-mentioned product for the manufacturer JULPHAR because it is not complying with standard specification and it has quality defect regarding to Julphar Scientific Office.
The product has the scientific name (Ibuprofen), registration no (98-186-74) and batch no (621). Therefore, SFDA obliged the manufacturer to withdraw the batch number from the markets.

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  • Call Centre 19999


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