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Article R5121-5-2 of the French Public Health Code

Except where there is a risk to patients’ health, the proprietary medicinal products mentioned in b of 5° of Article L. 5121-1 which are presented in a modified-release oral pharmaceutical form different from that of the reference proprietary medicinal product are identified by a decision of the Director General of the Agence nationale de sécurité du médicament et des produits de santé mentioning the corresponding reference proprietary medicinal product. This…

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Article R5121-6 of the French Public Health Code

Generic groups without a reference medicinal product, as provided for in Article L. 5121-1, are created in the register of generic groups by decision of the Director General of the Agence nationale de sécurité du médicament et des produits de santé. For the purposes of applying these provisions, the Ministers responsible for health and social security, at the request of an applicant, may refer to the Director General of the…

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Article R5121-7 of the French Public Health Code

A generic medicinal product or a medicinal product belonging to a generic group without a reference medicinal product, whose marketing authorisation is withdrawn, is removed from the register of generic groups. When the marketing authorisation of a generic medicinal product or of a medicinal product belonging to a generic group without a reference medicinal product is suspended, a reference to it is included in the register of generic groups for…

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Article R5121-8 of the French Public Health Code

The directory of generic groups lists the medicinal products included in each generic group, specifying their strength and pharmaceutical form. The generic groups are grouped by active substance designated by its common name preceded by the words “common name” and by route of administration. The information which, in application of article R. 5125-55, must be included in a prescription under a non-proprietary name is specified in the directory for the…

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Article R5121-9 of the French Public Health Code

Decisions to include a medicinal product in the register of generic groups, to amend these decisions and to remove a medicinal product from this register, governed by this section, are published on the website of the Agence nationale de sécurité du médicament et des produits de santé.

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Article R5121-9-1 of the French Public Health Code

The reference list of similar biological groups provided for in article L. 5121-10-2 is presented for each reference biological medicinal product for which the name, strength, pharmaceutical form and common name of the active substance it contains are indicated. This list includes the medicinal products included in each similar biological group within the meaning of b of 15° of article L. 5121-1 and specifies, for each of these medicinal products,…

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Article R5121-9-2 of the French Public Health Code

When a marketing authorisation is granted for a biological medicinal product which may be identified as a similar biological medicinal product, the Director General of the Agence nationale de sécurité des médicaments et des produits de santé : 1° Identifies it as a similar biological medicinal product, mentioning the corresponding reference medicinal product, by means of a decision, which may include recommendations and warnings, and which he notifies to the…

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Article R5121-9-3 of the French Public Health Code

The Director General of the Agence nationale de sécurité des médicaments et des produits de santé: 1° Suspends or withdraws the decision referred to in 1° of Article R. 5121-9-2 identifying a similar biological medicinal product in the event of non-renewal, suspension, withdrawal or lapse of the marketing authorisation for this medicinal product; 2° Removes the similar biological medicinal product from the reference list of similar biological groups in the…

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