Drug product selection definition

Drug product selection means the act of selecting the source of supply of a drug product.
Drug product selection means the interchange for a prescribed pharmaceutical product in accordance with Section
Drug product selection means the interchange for a prescribed pharmaceutical product in accordance with Section 25 of this Act and Section 3.14 of the Illinois Food, Drug and Cosmetic Act.

Examples of Drug product selection in a sentence

  • Drug product selection will result in a lower cost to the purchaser.

  • The dispensing pharmacy shall be responsible for packaging and labeling leave and release drugs in compliance with this paragraph.15.8(9) Drug product selection.

  • Drug product selection is allowed only between therapeutic equivalent drugs.

  • Drug product selection will be allowed for medicaid patients unless indicated in the prescriber's own handwriting on the face of the prescription or drug order "BRAND MEDICALLY NECESSARY".

  • Drug product selection means the act of selecting the brand or supplier of therapeutically equivalent generic drug products and will be permitted in the state of Idaho.

  • Drug product selection, with regard to an individual medical order, in accordance with the Nebraska Drug Product Selection Act.(3) The director shall, with the recommendation of the board, waive any of the limitations in subsection (2) of this section for purposes of a scientific study of the role of pharmacy technicians approved by the board.

  • Section 155A.32, Code 2017, is amended to read as29 follows:30 155A.32 Drug product selection —— restrictions.31 1.

  • Professional functions associated with the practice of pharmacy include: (a) The interpretation and evaluation of the prescription (b) Drug product selection (c) The compounding, dispensing, safe storage, and distribution of drugs and devices.

  • Biliary excretion of drugs.5. Bioavailability and Bioequivalence: Definitions of different parameters relative to bioavailability; purpose of bioavailability, relative and absolute bioavailability, methods of assaying bioavailability, criteria for bioequivalence studies.6. Drug product selection on the basis of bioavailability testing.

  • Basic skills in health system pharmacy, including goals and requirements of unit-dose medication systems.b. Common medication errors and prevention strategies.c. Mathematical calculations and medical abbreviations.d. Drug product selection policies and safeguards.e. A comprehensive examination.


More Definitions of Drug product selection

Drug product selection means the selection of a therapeutically equivalent drug, including a generic version for the prescribed brand, a branded version for the prescribed generic, a generic version by one (1) manufacturer for a generic version by a different manufacturer.
Drug product selection means the interchange for a

Related to Drug product selection

  • Drug Product means a specific drug in dosage form from a known source of manufacture, whether

  • Finished Product means a cannabis product in its final form to be sold at a retail premises.

  • Licensed Product means any method, process, composition, product, service, or component part thereof that would, but for the granting of the rights set forth in this Agreement, infringe a Valid Claim contained in the Licensed Patents.

  • Aerosol product means a pressurized spray system that dispenses product ingredients by means of a propellant contained in a product or a product's container, or by means of a mechanically induced force. “Aerosol Product” does not include “Pump Spray.”

  • Licensed Compound means (a) 3,4-Diaminopyridine, the chemical structure of which is set forth on Exhibit B-2; and (b) any derivatives, isomers, metabolites, prodrugs, acid forms, base forms, salt forms, or modified versions of such compound in (a).

  • Covered Product The consumer product that You purchased concurrently with and is covered by this Agreement.

  • Participating Product means any of the Breville products listed in the table below by model name and number that are supplied by Breville in Australia and sold directly by Breville or by a Participating Retail Store:

  • Biosimilar Product means, with respect to a Licensed Product in any country, any biosimilar product sold by a Third Party not authorized by or on behalf of Celgene, its Affiliates or Sublicensees, (a) that is a biosimilar biological product, as defined in 21 USC 379j-51 (or any successor or replacement thereof), a similar biological medicinal product, as defined in Annex I to Directive 2001/83/EC (or any successor or replacement thereof), or any similar biosimilar or generic product under the Laws of any country or jurisdiction, or (b) regarding which Regulatory Approval is obtained by referencing Regulatory Data of such Licensed Product.

  • 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;

  • Diagnostic Product means In Vitro Diagnostics, In Vivo Diagnostic Agents and any other aptamer product used for Diagnosis. For purposes of clarity, the term Diagnostic Product shall not include a product used for the delay of onset or progression of, or treatment or prevention of, an Indication.

  • Product means any deliverable under the Contract, which may include commodities, services, technology or software.

  • Tobacco product manufacturer means an entity that after the date of enactment of this Act directly (and not exclusively through any affiliate):

  • 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.

  • Covered Products means Your Applications, Libraries, Passes, Safari Extensions, Safari Push Notifications, and/or FPS implementations developed under this Agreement.

  • Aerosol coating product means a pressurized coating product containing pigments or resins that dispenses product ingredients by means of a propellant, and is packaged in a disposable can for hand-held application, or for use in specialized equipment for ground traffic/marking applications.

  • Product Labeling means, with respect to a Licensed Product in a country or other jurisdiction in the Territory, (a) the Regulatory Authority-approved full prescribing information for such Licensed Product for such country or other jurisdiction, including any required patient information, and (b) all labels and other written, printed, or graphic matter upon a container, wrapper, or any package insert utilized with or for such Licensed Product in such country or other jurisdiction.

  • Licensed Compounds means any EZH2 Compound(s) that is: