FDA will periodically update a publicly available list of MUMS-designated drugs. This list will be placed on file at the FDA Dockets Management Staff, and will contain the following information for each MUMS-designated drug:

1. (a) The name and address of the sponsor;
2. (b) The established name and trade name, if any, of the drug;
3. (c) The dosage form of the drug;
4. (d) The species and the proposed intended use for which MUMS-drug designation was granted; and
5. (e) The date designation was granted.

[72 FR 41017, July 26, 2007, as amended at 88 FR 45066, July 14, 2023]