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

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

Warning Date
2017-10-03
Warning Reason
Correction Actions
Advices to Consumer


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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