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Md. Code Ann., Health-Gen. § 21-227

Known as the Maryland Food, Drug, and Cosmetic Act

The act spans §§ 21–21 (58 sections).

On a specific written request by the Secretary, the manufacturer, packer, or distributor of any prescription drug that is sold or distributed in this State shall give the Secretary:

(1) Any information that the manufacturer, packer, or distributor has about the biological availability and clinical performance of the drug; and

(2) Any comparative information that the manufacturer, packer, or distributor has about any drug, of the same established name, that is manufactured, packed, or distributed by another person.

Official source: Maryland General Assembly. Reproduced from public-domain Maryland statutes; confirm against the official source for the current text. Not legal advice.