Without prejudice to the provisions of Articles R. 5132-4 and R. 5132-29, a prescription expressed as a non-proprietary name pursuant to Article L. 5125-23 and as defined in Article R. 5121-1 must include at least :
1° The active ingredient of the medicinal product designated by its non-proprietary name ;
2° The strength of the active ingredient;
3° The route of administration and pharmaceutical form.
If the medicinal product prescribed contains several active ingredients, the prescription must indicate the common name and strength of each active ingredient under the conditions set out in 1° and 2° above. The combination of these different active ingredients is indicated by the insertion of a “+” sign between each active ingredient.
The information provided for in 1°, 2° and 3° is included in the register of generics provided for in article R. 5121-5 and in the database provided for in III of article 47 of law no. 2000-1257 of 23 December 2000 relating to the financing of social security.