§ 111465
59 words·~1 min read·
/ca/health-and-safety-code/111465A research copy — for the controlling text, always check the official state or federal source. Not legal advice.
A drug or device is deemed misbranded under the laws of this state if it is subject to regulations issued by the United States Food and Drug Administration relating to tamper-resistant packaging, as set forth in Parts 200, 211, 314, and 800 of Volume 21 of the Code of Federal Regulations, as amended, but is not in compliance therewith.