(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.
Structure Maryland Statutes
Title 21 - Food, Drugs, and Cosmetics
Subtitle 2 - Maryland Food, Drug, and Cosmetic Act
Section 21-216 - Adulterated Drugs and Devices
Section 21-217 - Misbranded Drugs and Devices -- in General
Section 21-218 - Additional Grounds of Drug Misbranding
Section 21-220 - Prescription Requirements
Section 21-222 - Construction of 21-220 and 21-221
Section 21-223 - New Drugs -- in General
Section 21-224 - New Drugs -- Exemption When Intended for Investigational Use Only
Section 21-225 - New Drugs -- Inspection of Records
Section 21-226 - Printed Information for Use of Practitioners
Section 21-227 - Provision of Information on Request of Secretary