SFDA Suspends Registration and Recalls RABEZOLE Product due to its Lack of Bioequivalence with the Reference Product
2022-03-17
The Saudi Food and Drug Authority (SFDA) has issued a decision to recall and suspend the registration of the product (RABEZOLE) for the two registered strengths of 20 mg and 10 mg, (Registration No 95-368-07 and 96-368-07). The products are marketed by Jamjoom Pharmaceuticals. The decision has been taken as the product was found to be not bioequivalent with the reference product.