Nonpreferred drugs definition

Nonpreferred drugs means those drugs that were reviewed by the Pharmacy and Therapeutics Committee and not included on the preferred drug list. Nonpreferred drugs may be prescribed but require authorization prior to dispensing to the patient.
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Examples of Nonpreferred drugs in a sentence

  • Non-preferred drugs are usually not recommended as first line therapy and have alternative treatment modalities.

  • Non-preferred drugs in the listed classes require prior authorization.

  • Non-preferred drugs are brand-name drugs that are not on the Scripps Preferred Drug List.

  • For the specific settings and adjustments, users can refer Chapter Three.

  • Non-preferred drugs meet the definition of a covered outpatient drug and cannot be excluded from coverage.

  • The difference in cost betweenthe brand name drug and its generic equivalent will not count toward your annual out-of-pocket maximum.Retail or Mail order (30-day supply) Tier 1 generic: $10Preferred brand: $65 Non-preferred drugs: $90 (90-day supply)Tier 1 generic: $20 Preferred brand: $130 Non-preferred drugs: $180SpecialtyPreferred: $200Non-preferred: $400Bold text indicates significant plan changes.

  • Nonpreferred drugs are those that were reviewed by the Pharmacy and Therapeutics Committee and not included on the preferred drug list (PDL).

  • Applicable Drugs• Preferred drug(s): Inflectra, Renflexis• Non-preferred drug(s): Remicade, Avsola Non-Preferred Product Step Therapy CriteriaRemicade or Avsola may be covered when the criteria listed under Sections A., B., or C.

  • Nonpreferred drugs are those that were reviewed by the Pharmacy and Therapeutics Committee and not included on the preferred drug list.

  • Preferred Drug(s)/Product(s) Long-Acting (Neulasta, Udenyca, Fulphila, Ziextenzo, Nyvepria)Applicable Drugs• Preferred drug(s): Neulasta, Udenyca• Non-preferred drug(s): Fulphila, Nyvepria, Ziextenzo, Non-Preferred Product Step Therapy CriteriaFulphila, Nyvepria, or Ziextenzo may be covered when the criteria listed under Sections A., B., or C.

Related to Nonpreferred drugs

  • 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;

  • Covered drug means any prescription drug that:

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

  • Legend drugs means any drugs which are required by state

  • Narcotic drug means any of the following, whether produced directly or indirectly by extraction from substances of vegetable origin, or independently by means of chemical synthesis, or by a combination of extraction and chemical synthesis:

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

  • Invalid Drug Test means the result of a drug test for an oral fluid specimen that contains an unidentified adulterant, or an unidentified substance, that has abnormal physical characteristics, or that has an endogenous substance at an abnormal concentration preventing the laboratory from completing or obtaining a valid drug test result.

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

  • Legend drug or "prescription drug" means any drug or device that has been determined to be unsafe for self- medication or any drug or device that bears or is required to bear the legend:

  • Hospital system means a hospital and one or more

  • Drug addiction means a disease characterized by a

  • Biologics License Application or “BLA” means an application requesting permission from the FDA to introduce, or deliver for introduction, a biological product into interstate commerce, or any similar application or submission for marketing authorization of a product filed with a Regulatory Authority to obtain Regulatory Approval for such product in a country or group of countries.

  • FDA Act means the U.S. Federal Food, Drug, and Cosmetic Act, as amended.

  • Criminal drug statute means a Federal or non-Federal criminal statute involving the manufacture, distribution, dispensing, possession or use of any controlled substance.

  • New Drug Application means a new drug application in the United States for authorization to market a product, as defined in the applicable laws and regulations and submitted to the FDA.

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

  • Generic Drug means a Prescription Drug that is medically equivalent to a Brand Name Drug as determined by the FDA. It meets the same standards as a Brand Name Drug for purity, safety, strength and effectiveness and is manufactured and sold under its chemical, common, or official name.

  • Specialty Drugs means high-cost injectables, infused, oral, or inhaled Prescription Drugs for the ongoing treatment of a chronic condition, including but not limited to, the following: Hemophilia, Hepatitis C, Multiple Sclerosis, Rheumatoid Arthritis, Psoriasis, Crohn’s Disease, Cancer (oral medications), and Growth Hormones. These Prescription Drugs usually require specialized handling (such as refrigeration). Spouse means a person of the same or opposite sex who is legally married to Subscriber under the laws of the state or jurisdiction in which the marriage took place. A marriage legally entered into in another jurisdiction will be recognized as a marriage in the District of Columbia.

  • FDCA shall have the meaning ascribed to such term in Section 3.1(hh).

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

  • 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;

  • Food and food ingredients means substances, whether in liquid, concentrated, solid, frozen, dried, or dehydrated form, that are sold for ingestion or chewing by humans and are consumed for their taste or nutritional value. Food and food ingredients do not include alcoholic beverages and tobacco.

  • Infectious Disease means an illness that is capable of being spread from one individual to another.

  • Pre-Licensed Therapist means an individual who has obtained a Master’s Degree in Social Work or Marriage and Family Therapy and is registered with the BBS as an Associate CSW or MFT Intern acquiring hours for licensing. An individual’s registration is subject to regulations adopted by the BBS.

  • Biological Samples means any physical samples obtained from Study Participants in accordance with the Protocol for the purposes of the Study.

  • Chemical dependency means the physiological and psychological addiction to a controlled drug or substance, or to alcohol. Dependence upon tobacco, nicotine, caffeine or eating disorders are not included in this definition.