Medicinal drugs definition

Medicinal drugs or “drugs” means those substances or preparations commonly known as “prescription” or “legend” drugs which are required by federal or state law to be dispensed only on a prescription, but shall not include patents or proprietary preparations as hereafter defined.
Medicinal drugs. ’ or ‘‘Drugs’’ means ‘‘those substances or preparations commonly known as ‘prescription’ or ‘legend’ drugs which are required by federal or state law to be dispensed only on a prescription ’’ Fla. Stat. Ann. 465.003(8).
Medicinal drugs means a substance or preparation commonly known as a 'prescription' or 'legend' drug which is required by law to be dispensed only under

Examples of Medicinal drugs in a sentence

  • Medicinal drugs may be dis- pensed in a Class II institutional pharmacy, but only in accordance with the provisions of this section.

  • Basic Outpatient Special conditionsDrugs (medically prescribed)▪ Medicinal drugs authorized for use for the indication concerned by Swissmedic, the Swiss Agency for Therapeutic Products No contributions are made for preparations on the List of Pharmaceutical Preparations Paid for by Insureds (LPPV) and for drugs on Visana’s list of durgs (cf.

  • Medicinal drugs are commonplace in health care settings, and some have been found to cause or exacerbate asthma, mostly in occupational settings.

  • Medicinal drugs and driving among Spaniards: Data from national survey.

  • Medicinal drugs such as painkillers etc., will not be issued or administered by any person (including trained first aiders) to any other person, with the exception of students who rely on this type of support.

  • Medicinal drugs also represent a major challenge in achieving the desirable standards of quality, level of accessibility, and quality of use.

  • Additional fees may apply.• Medicinal drugs such as diet pills, inhalers, cough syrup, and pain pills may cause a preliminary positive result.• The tests may yield preliminary positive results with prescription drugs such as tricyclic antidepressants, barbiturates, benzodiazepine, methadone, buprenorphine (including Subutex, Suboxone, Temgesic,Buprenex, Norspan, and Butrans), and opiates (including morphine, hydrocodone, Oxycodone, and codeine) are ingested, even at therapeutic doses.

  • Medicinal drugs are permitted if provided by parents/carers, or if urgent medical attention is provided in line with the agreed terms and conditions of signing into the Academy.

  • Medicinal drugs are most prevalent in Belgium (2.99%) and Portugal (2.84%).

  • Medicinal drugs, when they are of good quality, accessible to patients, and used wisely, are arguably one of the major contributors to good health and the general well being of society.

Related to Medicinal drugs

  • medicinal product means any substance or combination of substances presented for treating or preventing disease in human beings or animals and any substance or combination of substances which may be administered to human beings or animals with a view to making a medical diagnosis or to restoring, correcting or modifying physiological functions in humans or in animals;

  • Drug addiction means a disease characterized by a

  • Biological Samples means any physical samples obtained from Study Participants in accordance with the Protocol for the purposes of the Study.

  • Collaborative drug therapy management means participation by an authorized pharmacist and a physician in the management of drug therapy pursuant to a written community practice protocol or a written hospital practice protocol.

  • Clinical laboratory means a facility for the microbiological, serological, chemical, hematological, radiobioassay, cytological, immunohematological, pathological, or other examination of materials derived from the human body for the purpose of providing information for the diagnosis, prevention, or treatment of a disease or assessment of a medical condition.

  • Collaborative pharmacy practice means a practice of pharmacy whereby one or more pharmacists have jointly agreed, on a voluntary basis, to work in conjunction with one or more practitioners under protocol whereby the pharmacist may perform certain pharmaceutical care functions authorized by the practitioner or practitioners under certain specified conditions or limitations.

  • FDA means the United States Food and Drug Administration and any successor agency thereto.

  • cosmetic product means any substance or mixture intended to be placed in contact with the external parts of the human body (epi­ dermis, hair system, nails, lips and external genital organs) or with the teeth and the mucous membranes of the oral cavity with a view exclusively or mainly to cleaning them, perfuming them, changing their appearance, protecting them, keeping them in good condition or correcting body odours;

  • Prescription drug order means an original or new order from a practitioner for drugs, drug-related devices or treatment for a human or animal, including orders issued through collaborative care agreements. Lawful prescriptions result from a valid practitioner-patient relationship, are intended to address a legitimate medical need, and fall within the prescribing practitioner's scope of professional practice;

  • cGMP means current Good Manufacturing Practices as specified in the United States Code of Federal Regulations, ICH Guideline Q7A, or equivalent laws, rules, or regulations of an applicable Regulatory Authority at the time of manufacture.

  • Bulk drug substance means any substance that is represented for use, and that, when used in the

  • Tobacco product means any substance containing tobacco leaf, including but not limited to, cigarettes, cigars, pipe tobacco, hookah tobacco, snuff, chewing tobacco, dipping tobacco, bidis, blunts, clove cigarettes, or any other preparation of tobacco; and any product or formulation of matter containing biologically active amounts of nicotine that is manufactured, sold, offered for sale, or otherwise distributed with the expectation that the product or matter will be introduced into the human body by inhalation; but does not include any cessation product specifically approved by the U.S. Food and Drug Administration for use in treating nicotine or tobacco dependence.

  • Criminal drug statute means a Federal or non-Federal criminal statute involving the manufacture, distribution, dispensing, possession or use of any controlled substance.

  • Vaccine means a specially prepared antigen which, upon administration to a person, will result in immunity and, specifically for the purposes of this rule, shall mean influenza and pneumococcal vaccines.

  • GMP means the amount proposed by Contractor and accepted by Owner as the maximum cost to Owner for construction of the Project in accordance with this Agreement. The GMP includes Contractor’s Construction Phase Fee, the General Conditions Cost, the Cost of the Work, and Contractor’s Contingency amount.