The following shall be removed from the list mentioned in article R. 5126-58:
1° A medicinal product which ceases to fulfil the condition mentioned in 1°, 2° or 3° of article R. 5126-59. This deletion is carried out automatically and without prior notification of the authorisation holder or the company responsible for its operation or parallel distribution;
2° A medicinal product registered pursuant to 2° of Article R. 5121-58, at the request of the Ministers, after prior notification under the conditions set out in Article R. 5126-62 of the authorisation holder or the company responsible for its operation or parallel distribution;
3° A medicinal product which ceases to meet the criteria set out in 1° of Article R. 5126-58, after prior notification under the conditions set out in Article R. 5126-62 to the holder of the authorisation or the company responsible for its operation or parallel distribution.