Prescription Drug Program definition

Prescription Drug Program means prescription drug program services provided to a Sponsor pursuant to an agreement with ESI, including any Formulary.
Sample 1Sample 2Sample 3
Prescription Drug Program means the prescription drug services and benefits specified by Sponsor which are provided to Members under this Agreement.
Sample 1Sample 2
Prescription Drug Program means the Card Program provided by LTCPA under the Medicare Statute.
Sample 1Sample 2

Examples of Prescription Drug Program in a sentence

  • The Board shall provide a prescription drug benefit for Cigna OAP and Cigna OAPIN plan members, as well as a mail order Prescription Drug Program for the purchase of maintenance type prescription drugs, including insulin and related supplies.

  • The State administered Prescription Drug Program shall be continued in keeping with the legislative appropriation.

  • COB does not apply to the Outpatient Prescription Drug Program Bene­ fits.

  • In certain situations, you will have to file your own Claims in order to obtain benefits under the Outpatient Prescription Drug Program.

  • The 90‐Day Supply Prescription Drug Program provides delivery of Covered Drugs directly to your home address.

  • An eligible retiree, and the person who is said retiree’s spouse at the time of retirement, covered by the traditional Blue Cross/Blue Shield indemnity health care plan will be enrolled in the Preferred Rx Managed Prescription Drug Program.

  • This extension of benefits does not apply to the benefits provided in the following Benefit Section(s) of this Certificate: • Outpatient Prescription Drug Program Benefits CONTINUATION COVERAGE RIGHTS UNDER COBRA NOTE: Certain employers may not be affected by CONTINUATION OF COV­ ERAGE RIGHTS UNDER COBRA.

  • In addition to the benefits described in this benefit section, your coverage includes benefits for Maintenance Drugs and dia­ betic supplies obtained through the 90‐Day Supply Prescription Drug Program.

  • For information about the Mail Service Prescription Drug Program, Members may visit xxx.xxxxxxxxxxxx.xxx or call Customer Service.

  • The Board shall provide a prescription drug benefit for plan members, as well as a mail order Prescription Drug Program for the purchase of maintenance type prescription drugs, including insulin and related supplies.


More Definitions of Prescription Drug Program

Prescription Drug Program means any group or individual plan, policy, agreement or other arrangement sponsored or issued by a Plan Sponsor and administered by MAKORX pursuant to an agreement between the parties, which includes pharmacy services or benefits related to utilization of pharmaceutical products and any Formulary.
Sample 1
Prescription Drug Program. A program to manage pharmacy benefits for a Plan Sponsor pursuant to an Agreement with ProCare.
Sample 1
Prescription Drug Program means the specific pharmacy benefit management services and benefit design adopted by, and applicable to, Client under this Agreement.
Sample 1
Prescription Drug Program. A program to manage pharmacy benefits for a Plan Sponsor pursuant to an Agreement with MC-Rx. Programs: Includes, but are not limited to mandatory generic substitution, maximum allowable edits (i.e. quantity limits, step edits, prior authorization, etc.), Coordination of Benefits (COB), Drug Utilization Review (DUR), network compliance, formulary compliance, and eligibility verification.
Sample 1
Prescription Drug Program means any group or individual plan, policy, agreement or other arrangement sponsored, issued, or administered by a Sponsor, which includes pharmacy services or benefits related to utilization of pharmaceutical products and any Formulary. Sponsor may amend its Prescription Drug Program at any time, in its sole discretion, and such amendment shall not require the consent of Provider.
Sample 1

Related to Prescription Drug Program

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

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

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

  • 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.

  • 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;

  • 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.

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

  • Drug abuse means any pattern of pathological use of drugs that causes impairment in social or occupational functioning, or that produces physiological dependency evidenced by physical tolerance or by physical symptoms when it is withdrawn.

  • Participating Clinical Laboratory means a Clinical Laboratory 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.

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

  • Prescription means an order for drugs or medical supplies, written or signed or transmitted by word

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

  • PDMA means the Prescription Drug Marketing Act of 1987, as amended from time to time, together with any rules or regulations promulgated thereunder.

  • Treatment program means an abstinence based program or facility that is accredited by any of the following:

  • 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

  • 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.

  • Prescription device means an instrument, apparatus, implement, machine,

  • Phase III Clinical Trials means a Clinical Trial for the Product on sufficient numbers of patients to generate safety and efficacy data to support Regulatory Approval in the proposed therapeutic indication, conducted in accordance with current good clinical practices and in accordance with a protocol that has been reviewed by the FDA and reflects any comments or concerns raised by the same.

  • 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:

  • E-Verify Program above means the employment verification program administered by the United States Department of Homeland Security, the Social Security Administration, or any successor program.

  • HCFA means the United States Health Care Financing Administration and any successor thereto.

  • Phase I Clinical Trial means a study in humans which provides for the first introduction into humans of a product, conducted in normal volunteers or patients to generate information on product safety, tolerability, pharmacological activity or pharmacokinetics, or otherwise consistent with the requirements of U.S. 21 C.F.R. §312.21(a) or its foreign equivalents.

  • Drug Master File or “DMF” is described in 21 C.F.R. Part 314.420. A DMF is a submission to the FDA that may be used to provide confidential detailed information about facilities, processes, or articles used in the manufacturing, processing, packaging, and storing of one or more human drugs.

  • Phase 2 Clinical Trial means a human clinical trial of a product in any country that would satisfy the requirements of 21 C.F.R. 312.21(b) and is intended to explore a variety of doses, dose response, and duration of effect, and to generate initial evidence of clinical safety and activity in a target patient population, or a similar clinical study prescribed by the relevant Regulatory Authorities in a country other than the United States.

  • ERCOT Protocols means the document adopted by ERCOT, including any attachments or exhibits referenced in that document, as amended from time to time, that contains the scheduling, operating, planning, reliability, and Settlement (including Customer registration) policies, rules, guidelines, procedures, standards, and criteria of ERCOT. For the purposes of determining responsibilities and rights at a given time, the ERCOT Protocols, as amended in accordance with the change procedure(s) described in the ERCOT Protocols, in effect at the time of the performance or non-performance of an action, shall govern with respect to that action.

  • Phase III Clinical Trial means a large, controlled or uncontrolled Clinical Study that would satisfy the requirements of 21 CFR 312.21(c), intended to gather the additional information about effectiveness and safety that is needed to evaluate the overall benefit-risk relationship of the drug and to provide an adequate basis for physician labeling.