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Current as of January 01, 2025 | Updated by Findlaw Staff
(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.
Cite this article: FindLaw.com - Maryland Code, Health-General § 21-226 - last updated January 01, 2025 | https://codes.findlaw.com/md/health-general/md-code-health-gen-sect-21-226/
FindLaw Codes may not reflect the most recent version of the law in your jurisdiction. Please verify the status of the code you are researching with the state legislature before relying on it for your legal needs.
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