Current with changes from the 2024 Legislative Session
Section 21-226 - Printed information for use of practitioners(a) The manufacturer, packer, or distributor of any prescription drug that is sold or distributed in this State shall: (1) Keep correct copies of any printed matter that is:(i) Required to be included in any package in which the drug is sold or distributed; or(ii) Approved under the federal act; and(2) Send copies of the printed matter to any health practitioner who is authorized to administer the drug and who makes a written request for information about the drug.(b) This section does not exempt any person from any labeling requirement imposed under any other provision of this subtitle.