Drug Plan Formulary definition

Drug Plan Formulary means and refer to a standard listing of Covered pharmaceutical products, quantity limits, and clinical guidelines for determining coverage of such products developed by and periodically revised by SOUTHERN SCRIPTS and/or Plans.
Sample 1Sample 2Sample 3

Examples of Drug Plan Formulary in a sentence

  • Drugs Covered Under the Quebec Universal Drug Plan Formulary Drugs not covered under the group plan but listed in the Quebec Universal Drug Plan formulary, will be reimbursed in accordance with the Quebec Universal Drug Plan.

  • Dispense, without the authority of the prescribing physician, Ratio, PMS and Apotex brands of Amlodipine 5 mg when those brands were not designated as the Standing Offer Contract (SOC) product as required under the Saskatchewan Ministry of Health Drug Plan Formulary.

  • Dispense, without the approval and proper authority of the pre- scriber Mylan brand of Amlodipine 5 mg when that brand were not designated as the Standing Offer Contract (SOC) product as required under the Saskatchewan Ministry of Health Drug Plan Formulary.

  • Further tilting international investment rules in favor of investors at the expense of the ability of governments to regulate in the public interest is a threat to good governance and public welfare.

  • Without the approval and proper authority of the prescriber he dis- pensed on numerous and several occasions, Mylan brand of Amlodi- pine 5 mg when that brand was not designated as the Standing Offer Contract (SOC) product as required under the Saskatchewan Ministry of Health Drug Plan Formulary.

  • Without the approval of the prescribing physician, the Respondents dispensed on numerous and several occasions, Sandoz brand when that brand was not designated as the Standing Offer Contract (SOC) product as required under the Saskatchewan Ministry of Health Drug Plan Formulary.

  • Additional current design information is available in Appendix N - APS 2022 Prescription Drug Plan Formulary and in Appendix O - APS 2022 Additional Drug Coverage List.

  • Centers for Medicare & Medicaid Services, “Prescription Drug Plan Formulary, Pharmacy Network, and Pricing Information Files for Download,” webpage, June 14, 2022.

  • APS 2002 Prescription Drug Plan Formulary (also referred to in Information Item One as Attachment One) 2) Appendix O.

  • Because there is plan and formulary entry, exit, and re-design year to year, we treat each plan-year as a distinct plan and each formulary-year as a distinct formulary; for convenience we refer to each simply as a “plan” or a “formulary” rather than a plan-year or a formulary-year.5Specifically, we use the “Prescription Drug Plan Formulary, Pharmacy Network, and Pricing Informa- tion” files, also known as PUF or Pulic Use Files.

Related to Drug Plan Formulary

  • Commercialization Plan has the meaning set forth in Section 6.2.

  • Basic health plan model plan means a health plan as required in RCW 70.47.060(2)(e).

  • Marketing Plan means a plan or system concerning a material aspect of conducting business. Indicia of a marketing plan include any of the following:

  • Number of Students Who Began Program means the number of students who began the program who are scheduled to complete the program within the reporting calendar year.

  • Educational program means a program for educating and preparing physician assistants which is approved by the board.

  • Participating Prescription Drug Provider means an independent retail Pharmacy, chain of retail Pharmacies, mail-order Pharmacy or specialty drug Pharmacy which has entered into an agreement to provide pharmaceutical services to participants in the benefit program. A retail Participating Pharmacy may or may not be a select Participating Pharmacy as that term is used in the Vaccinations Obtained Through Participating Pharmacies section.

  • Number of Students Who Began the Program means the number of students who began a program who were scheduled to complete the program within 100% of the published program length within the reporting calendar year and excludes all students who cancelled during the cancellation period.

  • Flexi Plan means any individual indemnity hospital insurance plan under the VHIS framework with enhancement(s) to any or all of the protections or terms and benefits that the Standard Plan provides to the Policy Holder and the Insured Person, subject to certification by the Government. Such plan shall not contain terms and benefits which are less favourable than those in the Standard Plan, save for the exception as may be approved by the Government from time to time.

  • Prescription monitoring program means the electronic system within the Department of Health Professions that monitors the dispensing of certain controlled substances.

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

  • Procurement Plan means the Recipient’s procurement plan for the Project, dated April 2, 2010, and referred to in paragraph 1.16 of the Procurement Guidelines and paragraph 1.24 of the Consultant Guidelines, as the same shall be updated from time to time in accordance with the provisions of said paragraphs.

  • Development Plans has the meaning set forth in Section 3.2.

  • Program Plan means the tobacco settlement program plan dated February 14, 2001, including exhibits to the program plan, submitted by the authority to the legislative council and the executive council, to provide the state with a secure and stable source of funding for the purposes designated by section 12E.3A and other provisions of this chapter.

  • Marketing program means a program established by order of the director pursuant to this act prescribing rules and regulations governing the marketing for processing, distributing, selling, or handling an agricultural commodity produced in this state or agricultural commodity input during a specified period and

  • Development Plan has the meaning set forth in Section 3.2.

  • Prescription drugs means drugs, medicine and controlled substances which by law can only be prescribed for human use by persons authorized by law.

  • Participating Retail Health Clinic means a Retail Health Clinic which has a written agreement with the Claim Administrator or another Blue Cross and/or Blue Shield Plan to provide services to you at the time services are rendered.

  • Supply Plan has the meaning set forth in the CAISO Tariff.

  • 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.

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

  • Program of study means a curriculum that requires a candidate to demonstrate and document competency in the specific knowledge, skills, and dispositions for a particular endorsement to an educator’s license, a licensure content area, or level of licensure, and is:

  • Quality Plan means the quality plan to be produced by the Contractor in accordance with Schedule S2-10 (Quality Plan);

  • AML Program has the meaning ascribed thereto in Schedule 2.1(F)(8) hereof.

  • Training program means a standardized medication

  • Safety Plan means a written document that has procedures, requirements, or standards related to safety which the pool staff shall follow. The safety plan shall include training and emergency response procedures.

  • layout plan means a plan of the project depicting the division or proposed division of land into plots, roads, open spaces, amenities, etc. and other details as may be necessary;