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The CBG Medicines Data Bank includes the most important information on all medicinal products authorised for marketing in the Netherlands, including the SmPC, the (scientific) product information on a medicinal product; a more extensive package leaflet for the benefit of health professionals such as the prescribing doctor and the pharmacist, containing information regarding the safe and proper use of a medicinal product. Unfortunately, this information is only available in Dutch. The patient information leaflet is also available as well as a public assessment report for a number of products, which includes the scientific basis on which approval for a marketing authorisation or variation has been granted.

In the search results and overviews SmPCs in English can be found. Medicinal products with English texts are authorised in the Netherlands, but not marketed at the moment.

The basic data on medicinal products that have been authorised in the Netherlands following a European procedure can also be found here. Not only all allopathic medicinal products, but also all authorised homeopathic medicinal products are included. The MEB has had the task of assessing homeopathic medicinal products since 1996. Prior to 1996, these products were exempt from authorisation. Not all homeopathic medicinal products have been authorised (for further information see the Homeopathy section).

Various search parameters can be used to retrieve information. The data bank is updated on a weekly basis. A revised version presenting the most up-to-date situation can be found on the website every Thursday morning.

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Parallel (//) and identical (=)

Parallel imported products have a combined number: The RVG number is followed by two slanting lines // and the number of the original product. Products for which the composition, manufacturer, method of manufacture and analytical methods are identical to those of a previously authorised pharmaceutical product also have a combined number: the RVG number is followed by two horizontal lines = and the number of the identical authorised product.

For parallel medicinal products the SmPC of the original product is shown; for the exact composition and specific product information of the parallel product we refer to the package leaflet.

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