Model Drug definition

Model Drug means any Applicable Drug of the Manufacturer that is, or contains, a drug classified as insulin in American Hospital Formulary Service (AHFS) Drug Information or the DRUGDEX Information System compendia.
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Examples of Model Drug in a sentence

  • Plan Selected Model Drugs must include at least one Model Drug of each the following types of insulins: rapid-acting, short-acting, intermediate- acting, and long-acting.

  • Part D Sponsor’s Part D benefit will specify a copayment of no more than thirty-five dollars ($35) for a month’s supply of any Plan Selected Model Drug in the deductible, initial coverage, and coverage gap phases.

  • Plan Selected Model Drugs must include both the vial dosage form and pen dosage form for all Plan Selected Model Drugs, unless a Plan Selected Model Drug is not manufactured in both dosage forms.

  • Part D Sponsor may continue to offer a lower copay for a Plan Selected Model Drug at preferred or mail-order pharmacies in accordance with Part D program guidelines.

  • If Part D Sponsor covers a Plan Selected Model Drug in larger increments than a month’s supply, such as 2 or 3 month’s supply, the copayment on such increment must be equal to or less than the multiple of the month’s supply copayment (i.e., 2 times for 2 months and 3 times for 3 months) consistent with current CMS requirements.

  • The Part D Sponsor shall determine a month’s supply of any Plan Selected Model Drug in a manner consistent with how it determines month’s supplies of other Part D drugs.

Related to Model Drug

  • New drug means: (i) any drug, except a new animal drug or an animal feed bearing or containing

  • Prescription drug means any drug required by federal law or regulation to be dispensed only

  • MSAA Indicator Technical Specifications document means, as the context requires, either or both of the document entitled “Multi-Sector Service Accountability Agreement (MSAA) 2019-20 Indicator Technical Specifications November 5, 2018 Version 1.3” and the document entitled “Multi-Sector Service Accountability Agreement (MSAA) 2019-20 Target and Corridor-Setting Guidelines” as they may be amended or replaced from time to time;

  • Generic Drug means any Prescription Drug approved by the FDA that has the same bio-equivalency as a specific Brand Name Drug.

  • Brand Name Drug means a Prescription Drug that has been given a name by a manufacturer or distributor to distinguish it as produced or sold by a specific manufacturer or distributor and may be used and protected by a trademark.

  • Approved laboratory means a laboratory that is listed in the national conference of interstate milk shipments list of sanitation compliance and enforcement ratings distributed by the United States food and drug administration and as approved by the director.

  • Single tomogram system means a CT x-ray system which obtains x-ray transmission data during a scan to produce a single tomogram.

  • Multiple tomogram system means a computed tomography X-ray system which obtains X-ray transmission data simultaneously during a single scan to produce more than one tomogram.

  • Prescription drug order means a lawful order of a practitioner for a drug or device for a specific patient that is communicated to a pharmacist.

  • Automated drug dispensing system means a mechanical or electronic system that performs

  • Collaborative pharmacy practice means a practice of pharmacy whereby one or

  • Nonprescription drug or "over-the-counter drug" means any

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

  • Drug means (i) articles or substances recognized in the official United States Pharmacopoeia

  • Approved clinical trial means a phase I, phase II, phase III, or phase IV clinical trial that is conducted in relation to the prevention, detection, or treatment of cancer or other life-threatening disease or Condition and is described in any of the following:

  • Collaborative pharmacy practice agreement means a written and signed

  • Nonprescription drugs means nonnarcotic medicines or drugs which may be sold without a prescription and are prepackaged and labeled for use by the consumer in accordance with the requirements of the statutes and regulations of this state and the federal government;

  • 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.