Michigan Compiled Laws, Chapter 333. Health § 333.17704

Sec. 17704. (1) “Federal act” means the federal food, drug, and cosmetic act, 21 USC 301 to 399i.

(2) “Food and Drug Administration” or “FDA” means the United States Food and Drug Administration.

(3) “Generic name” means the established or official name of a drug or drug product.

(4) “Harmful drug” means a drug intended for use by human beings that is harmful because of its toxicity, habit-forming nature, or other potential adverse effect; the method of its use; or the collateral measures necessary to its safe and effective use and that is designated as harmful by a rule promulgated under this part.

(5) “Hormonal contraceptive patch” means a transdermal patch applied to the skin of an individual that releases a drug composed of a combination of hormones that is approved by the FDA to prevent pregnancy.

(6) “Interchangeable biological drug product” means either of the following, as applicable:

(7) “Internship” means an educational program of professional and practical experience for an intern.