Section 151.361 — Manufacturer Disclosure.
151.361 MANUFACTURER DISCLOSURE. Subdivision 1. After January 1, 1976. The manufacturer, packager, or distributor of any human use legend drug sold, delivered, or offered for sale in the state of Minnesota after January 1, 1976 must have printed on the label on the immediate container of the drug the name and address of the manufacturer […]
Section 151.37 — Legend Drugs; Who May Prescribe, Possess.
151.37 LEGEND DRUGS; WHO MAY PRESCRIBE, POSSESS. Subdivision 1. Prohibition. Except as otherwise provided in this chapter, it shall be unlawful for any person to have in possession, or to sell, give away, barter, exchange, or distribute a legend drug. Subd. 2. Prescribing and filing. (a) A licensed practitioner in the course of professional practice […]
Section 151.375 — Investigational Drug Use.
151.375 INVESTIGATIONAL DRUG USE. Subdivision 1. Title; citation. This section may be cited as the “Right to Try Act.” Subd. 2. Definitions. (a) For the purposes of this section, the following terms have the meanings given them. (b) “Eligible patient” means a patient who meets the requirements in subdivision 3. (c) “Investigational drug, biological product, […]
Section 151.29 — Violation A Misdemeanor.
151.29 VIOLATION A MISDEMEANOR. Any person violating any of the provisions of this chapter, or rules hereunder, shall be guilty of a misdemeanor, unless otherwise provided. History: (5808-30) 1937 c 354 s 30; 1985 c 248 s 70
Section 151.30 — County Attorney To Prosecute.
151.30 COUNTY ATTORNEY TO PROSECUTE. It shall be the duty of the county attorney of the county wherein any offense under this chapter is committed to prosecute the offender, except that when offenses hereunder are committed in cities of the first class it shall be the duty of the city attorney thereof to prosecute the […]
Section 151.301 — Reports To Commissioner Of Health.
151.301 REPORTS TO COMMISSIONER OF HEALTH. (a) The board shall maintain a record of an event that comes to the board’s attention that, in the judgment of the board or a committee of the board, qualifies as an adverse health care event under section 144.7065. (b) Within 30 days of making a determination under paragraph […]
Section 151.22 — Liability For Quality Of Drugs.
151.22 LIABILITY FOR QUALITY OF DRUGS. Every pharmacist in charge or proprietor of a pharmacy shall be responsible for the quality of all drugs, medicines, chemicals, and poisons procured for use and sold therein, except proprietary medicines or other articles sold in the original package of the manufacturer. History: (5808-23) 1937 c 354 s 23; […]
Section 151.23 — Poisons Must Be Labeled.
151.23 POISONS MUST BE LABELED. It shall be unlawful for any person to sell at retail any poison without affixing to the package or receptacle containing the same a label conspicuously bearing the word “poison,” and the name and the business address of the seller, and being satisfied that such poison is to be legitimately […]
Section 151.24 — Sale Of Poisons Must Be Recorded.
151.24 SALE OF POISONS MUST BE RECORDED. It shall be unlawful: (1) for any person, either acting independently or while in the employ of another, to sell or give away any poison, as designated by the board, without first recording in a book to be kept for that purpose with an indelible pencil or ink […]
Section 151.252 — Licensing Of Drug Manufacturers; Fees; Prohibitions.
151.252 LICENSING OF DRUG MANUFACTURERS; FEES; PROHIBITIONS. Subdivision 1. Requirements. (a) No person shall act as a drug manufacturer without first obtaining a license from the board and paying any applicable fee specified in section 151.065. (b) In addition to the license required under paragraph (a), each manufacturer required to pay the registration fee under […]