Drugs

Veterinary Products Law In Arab Gulf Cooperation Council Countries

2021-06-23
Veterinary Products Law In Arab Gulf Cooperation Council Countries
List
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Code Procedures of Importing and Exporting

2021-05-09
Code Procedures of Importing and Exporting
Guide
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Veterinary Incentive Project List

2026-03-29
Veterinary Incentive Project List
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"SFDA" Withdraws and Suspends the Registration of (Omiz Plus 20mg, 40mg)

The Saudi Food & Drug Authority (SFDA) has announced the withdrawal and suspension of registration of Omiz Plus 40/1100mg Capsule with registration number (244-277-12), and Omiz Plus 20/1100 mg Capsule with registration number (245-277-12).

SFDA added that, the medicines produced by Tabuk Pharmaceuticals.  

  • To report sector-related issues

  • Call Centre 19999

Other Warnings

All Warnings

Requirements for Clearance of Medicines, Pharmaceutical Preparations, Medical Devices , Medical Supplies and Food Supplies for the Use of Pilgrims

2026-04-01
Requirements for Clearance of Medicines, Pharmaceutical Preparations, Medical Devices , Medical Supplies and Food Supplies for the Use of Pilgrims
Procedural rule
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Investor Guide to Obtain Scientific Office Licensing

2019-04-14
Investor Guide to Obtain Scientific Office Licensing
Guide
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Guide for Investor to Obtain a Pharmaceutical Manufacturer License

2020-01-01
Guide for Investor to Obtain a Pharmaceutical Manufacturer License
Guide
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Extending Validity Period for Pharmaceutical Products

2020-04-06
Extending Validity Period for Pharmaceutical Products
Guide
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Warning Date
    2021-03-25

“SFDA” Suspends and Withdraws the Registration of (LORA S Tablet‎) and (LORINASE Tablet‎)

2021-03-25

The Saudi Food & Drug Authority (SFDA) has announced the withdrawal and suspension of registration of the pharmaceutical product (LORA S Tablet, batch number (8-968-15)) and (LORINASE TABLETS, batch number (250-212-09) ‎).

SFDA added that (LORA S Tablet‎) is marketed by Dammam Pharma Company, whether the other product (LORINASE Tablet‎)

  • To report sector-related issues

  • Call Centre 19999

Other Warnings

All Warnings
Warning Date
    2021-03-15

“SFDA” Withdraws and Suspends the Registration of Pharmaceutical Product “Proton”

2021-03-15

The Saudi Food & Drug Authority (SFDA) has announced the withdrawal and suspension of registration of the pharmaceutical product “PROTON 40mg E.C TABLET, batch number (134-212-01 &134-212-01) and “PROTON 20mg E.C TABLET, batch number (134-212-01 &135-212-01),

The Proton brand was manufactured by the Saudi Pharmaceutical Industries and Medical Appliances Corporation (SPIMACO)

  • To report sector-related issues

  • Call Centre 19999

Other Warnings

All Warnings
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