Approved Drug List definition

Approved Drug List means a list of both Generic and Preferred Brand Name Drugs, including Specialty Drugs, approved by Total Health Care USA Pharmacy and Therapeutics Committee for use by our Members. Preferred Brand Name Drugs are usually Brand Name Drugs that have been on the market for a while or are commonly prescribed and have been selected based on their clinical effectiveness and safety. Non-preferred Brand Name Drugs are usually the highest cost drugs in a given category that have lower-cost alternatives with equal or better clinical effectiveness.
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Approved Drug List means CalOptima’s continually updated list of medications and supplies that may be obtained without prior authorization.
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Approved Drug List means a list of both Generic and Preferred Brand Name Drugs, including Specialty Drugs. These have been approved by Total Health Care USA Pharmacy and Therapeutics Committee. Preferred Brand Name Drugs are usually Brand Name Drugs
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Examples of Approved Drug List in a sentence

  • Medications not included on the Approved Drug List shall require prior authorization by CalOptima.

  • County shall comply with the CalOptima Approved Drug List and its associated drug utilization or disease management guidelines and protocols.

  • CalOptima shall publish and maintain an Approved Drug List pursuant to CalOptima Policies.

  • CalOptima shall review prescriptions for medications not listed on the Approved Drug List in a timely manner.

  • Coverage is based on the Plan Approved Drug List (which may include Generic, Preferred Brand, and Non-Preferred Brand Drugs).

  • Coverage is based on the Plan Approved Drug List (which may include Generic, Preferred Brand and Non-Preferred Brand Drugs).

  • Approved Drug List (Formulary)Find CHA’s Drug Formulary on CHA’s website under Member Resources or follow the link below.

  • Drugs may be added or removed from the Approved Drug List throughout the Plan Year.Prescription Drug costs, including Copays, combine with medical costs toward your Maximum Out-of-Pocket Expenses.Covered Services (with a prescription):• Drugs that are meant to be self-administered, regardless of the setting as defined by the federal Food and Drug Administration, including Growth Hormone Therapy.

  • Drugs may be added or removed from the Approved Drug List throughout the Plan Year.Prescription Drug costs, including Co-pays, combine with medical costs toward your Maximum Out of Pocket Expenses.Covered Services (with a prescription):• Drugs that are meant to be self-administered, regardless of the setting as defined by the federal Food and Drug Administration, including Growth Hormone Therapy.

  • Drugs may be added or removed from the Approved Drug List throughout the Plan Year.Prescription Drug costs, including Copays, combine with medical costs toward your Maximum Out-of-Pocket Expenses.Covered Services (with a prescription):• Drugs that are meant to be self-administered, regardless of the setting, as defined by the federal Food and Drug Administration, including Growth Hormone Therapy.


More Definitions of Approved Drug List

Approved Drug List means a list of both Generic and Preferred Brand Name Drugs,
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Approved Drug List means a list of both Generic and Preferred Brand Name Drugs, including Specialty Drugs, approved by Total Health Care, USA Pharmacy and Therapeutics Committee for use by our Members. Preferred Brand Name Drugs are usually Brand Name Drugs that have been on the market for a while or are commonly prescribed and have been selected based on their clinical effectiveness and safety. Non-preferred Brand Name Drugs are usually the highest cost drugs in a given category that have lower-cost alternatives with equal or better clinical effectiveness.
Sample 1Sample 2
Approved Drug List means a list of both Generic and Preferred Brand Name Drugs, including Specialty Drugs. These have been approved by Total Health Care USA Pharmacy and Therapeutics Committee. Preferred Brand Name Drugs are usually Brand Name Drugs that have been on the market for a while or are commonly prescribed. They have been
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Related to Approved Drug List

  • 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.

  • New Drug Application or “NDA” means a New Drug Application filed with the FDA as described in 21 C.F.R. § 314, a Biological License Application (BLA) pursuant to 21 C.F.R. § 601.2, or any equivalent or any corresponding application for Regulatory Approval (not including pricing and reimbursement approval) in any country or regulatory jurisdiction other than the United States.

  • Drug addiction means a disease characterized by a

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

  • Approved List means Securities followed by the Global Fundamental Research Group and tracked on the Approved List. Securities may be added, removed, or undergo periodic ratings changes.

  • Prescription drug order means an order from a prescriber for a drug or device that is

  • 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.

  • 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:

  • Covered drug means any prescription drug that:

  • FFDCA means the United States Federal Food, Drug, and Cosmetic Act, 21 U.S.C. § 301 et seq., as amended from time to time, together with any rules, regulations and requirements promulgated thereunder (including all additions, supplements, extensions, and modifications thereto).

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

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

  • 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.

  • Generic Drug means a prescription drug approved under 21 U.S.C. § 355(j) or 42 U.S.C. 262(k).

  • 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 Approval Application means an application for Regulatory Approval required before commercial sale or use of a Product as a drug in a regulatory jurisdiction.

  • 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.

  • low protein modified food product means a food product that is specially formulated to have less than one gram of protein per serving and is intended to be used under the direction of a Practitioner for the dietary treatment of an inherited metabolic disease, but does not include a natural food that is naturally low in protein; and

  • Drug Application means a new drug application, an abbreviated drug application, or a product license application for any Product, as appropriate, as those terms are defined in the FDCA.

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

  • Relevant Electric Retail Regulatory Authority means an entity that has jurisdiction over and establishes prices and policies for competition for providers of retail electric service to end- customers, such as the city council for a municipal utility, the governing board of a cooperative utility, the state public utility commission or any other such entity.

  • Approved Vendor List means a list of approved vendors established under Section 63G-6a-507.

  • Legend drugs means any drugs which are required by state

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

  • Product Approval means the approval of a Governmental Authority necessary for the marketing and sale of the Product in a given country or regulatory jurisdiction, which may include the approval of an MAA (but shall not include any Pricing Approvals).

  • Federal work authorization program means any of the electronic verification of work authorization programs operated by the United States Department of Homeland Security or any equivalent federal work authorization program operated by the United States Department of Homeland Security to verify information of newly hired employees, pursuant to the Immigration Reform and Control Act of 1986 (IRCA), D.L. 99-603.