The package shall contain the data of medicinal products accumulated by the State Medicines Control Agency: name, active substance in the preparation, strength, pharmaceutical form and routes of administration of the medicinal product, group and subset of the medicinal product, need for prescription, state of monitoring and control, date of first registration and last re-registration, current stage of the medicinal product, name and country of the undertaking registering the product. The package shall also contain information on the packaging of medicinal products, such as the state, type and description of the packaging. The dataset consists of two tables: “medicinal product” (information on the medicinal product and its packaging) and “Phase of medicinal product” (information on changes in the stages of the medicinal product in time). In the first table, one line corresponds to one medicinal product and its packaging. One row of the second table contains information about a change in the stage of one medicinal product. Both tables can be combined through the product identification number (vid) column.