Maryland Statutes
Subtitle 2 - Maryland Food, Drug, and Cosmetic Act
Part III - Drugs and Devices

Section 21-216 - Adulterated Drugs and Devices - (a) For purposes of this subtitle, a drug or device...

Section 21-217 - Misbranded Drugs and Devices -- in General - (a) For purposes of this subtitle, a drug or device...

Section 21-218 - Additional Grounds of Drug Misbranding - (a) In this section, “antibiotic drug” means any drug that:...

Section 21-219 - Exemptions From Labeling and Packaging Requirements for Drugs and Devices Subject to Additional Processing, Labeling, or Packing - (a) A drug or device is not subject to the...

Section 21-220 - Prescription Requirements - (a) A drug that is intended for use by human...

Section 21-221 - Label Requirements for Prescription Drugs; Exemption From Provisions on Misbranded Drugs - (a) A drug that is dispensed under a prescription shall...

Section 21-222 - Construction of 21-220 and 21-221 - Nothing in § 21-220 or § 21-221 of this subtitle...

Section 21-223 - New Drugs -- in General - (a) This section does not apply to any drug that:...

Section 21-224 - New Drugs -- Exemption When Intended for Investigational Use Only - (a) (1) A new drug is not subject to the...

Section 21-225 - New Drugs -- Inspection of Records - Any person who is required under § 21-223 or §...

Section 21-226 - Printed Information for Use of Practitioners - (a) The manufacturer, packer, or distributor of any prescription drug...

Section 21-227 - Provision of Information on Request of Secretary - On a specific written request by the Secretary, the manufacturer,...