§ 21-226. Printed information for use of practitioners

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   (a) In general. -- 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) Construction of section. -- This section does not exempt any person from any labeling requirement imposed under any other provision of this subtitle.

HISTORY: An. Code 1957, art. 43, § 187B; 1982, ch. 240, § 2; 1987, ch. 306, § 2.

                    
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