Prescription drug or device definition

Prescription drug or device or "legend drug or device" means:
Prescription drug or device means a drug or device that is dispensed pursuant to the order of a practitioner.
Prescription drug or device means[:] an instrument, apparatus, implement, 803 machine, contrivance, implant, in vitro reagent, or other similar or related article, and any

Examples of Prescription drug or device in a sentence

  • A Prescription drug or device that may have a lower out-of-pocket cost than a Non-Preferred drug.

  • A Prescription drug or device that may have a higher out-of-pocket cost than a Preferred drug.

  • Prescription drug or device" means a drug or device that is dispensed pursuant to the order of a practitioner.HISTORY: 1999 Act No. 85, Section 1.

  • Prescription drug or device has the definition found in section 38-2841.

  • Prescription does not include a chart order.Section 20: Defines Prescription drug or device or legend drug or device: (a) A drug or device which is required under federal law to be labeled with one of statements listed in (i-iii) prior to being dispensed or delivered; or (b) a drug or device required by law to be dispensed pursuant only to a prescription or chart order or which is restricted to use by practitioners only.

  • Bill Summary SECTION 1The following definitions are included in Section 1: Claims Processing Services; Health Benefit Plan; Healthcare Insurer; Other Prescription drug or device services; Pharmacist; Pharmacy; Pharmacy Benefits Manager; Pharmacy Benefits Manager Affiliate;; Pharmacy Benefits Manager Network; Pharmacy Benefits Plan or program; Pharmacy Services Administrative Organization; and Rebate.


More Definitions of Prescription drug or device

Prescription drug or device means[:] an instrument, apparatus,

Related to Prescription drug or device

  • 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.

  • 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;

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

  • 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;

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

  • 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.

  • 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.

  • 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

  • New Drug Application or “NDA” means a new drug application filed with a Regulatory Authority (not including pricing and reimbursement approval), that is analogous to the new drug application with the United States Food and Drug Administration described in 21 C.F.R. § 314.

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

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

  • Investigational Medicinal Product means the study drug or control material as defined in the Protocol.

  • 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.

  • Biological safety cabinet means a containment unit suitable for the preparation of low to moderate risk agents where there is a need for protection of the product, personnel, and environment, according to National Sanitation Foundation (NSF) Standard 49.

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

  • 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.

  • in vitro diagnostic medical device means any medical device which is a reagent, reagent product, calibrator, control material, kit, instrument, apparatus, equipment, software or system, whether used alone or in combination, intended by the manufacturer to be used in vitro for the examination of specimens, including blood and tissue donations, derived from the human body, solely or principally for the purpose of providing information:

  • Legend drugs means any drugs which are required by state

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

  • Covered drug means any prescription drug that:

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

  • 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.

  • MHLW means the Japanese Ministry of Health, Labour and Welfare, and any successor agency thereto.

  • Licensed clinical social worker means an individual who meets the licensed clinical social worker requirements established in KRS 335.100.