Contraceptive Drugs definition

Contraceptive Drugs means all drugs approved by the FDA that are used to prevent pregnancy, including but not limited to, hormonal drugs administered orally, transdermally, and intravaginally.
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Contraceptive Drugs means all drugs approved by the United States
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Examples of Contraceptive Drugs in a sentence

  • Contraceptive Drugs, except for any above stated covered contraceptive services.

  • Contraceptive Drugs, except for any above stated covered contraceptive devices.

  • Benefits are not available under this benefit provision for contraceptive drugs and devices not listed on the Contraceptive Drugs & Devices List.

  • Hepatitis C virus (HCV) screening for persons at high risk for infectionThe FDA‐approved contraceptive drugs and devices currently covered under this benefit provision are listed on the Contraceptive Drugs & Devices List.

  • We care about everyone’s health, wellness & safety and try to halt possible errors, accidents or injuries from occurring.

  • Benefits are not available under this benefit provision forcontraceptive drugs and devices not listed on the Contraceptive Drugs & Devices List.

  • Allergy in­ jections are not considered immunizations under this benefit provision.The FDA‐approved contraceptive drugs and devices currently covered under this benefit provision are listed on the Contraceptive Drugs & Devices List.

  • Hepatitis C virus (HCV) screening for persons at high risk for infection The FDA approved contraceptive drugs and devices currently covered under this benefit provision are listed on the Contraceptive Drugs & Devices List.

  • Allergy injections are not considered immunizations under this benefit provision The FDA‐approved contraceptive drugs and devices currently covered under this benefit provision are listed on the Contraceptive Drugs & Devices List.

  • Contraceptive Drugs and Devices covered under the Outpatient Prescription Drug Benefit are not subject to the Member Calendar Year Brand Drug Deductible.

Related to Contraceptive Drugs

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  • Medical marijuana product means a product that contains cannabinoids that have been extracted from plant material or the resin therefrom by physical or chemical means and is intended for administration to a licensed patient, including but not limited to concentrates, oils, tinctures, edibles, pills, topical forms, gels, creams, and other derivative forms, except that this term does not include live plant forms.

  • Fluoroscopic imaging assembly means a subsystem in which X-ray photons produce a visual image. It includes the image receptor(s) such as the image intensifier and spot-film device, electrical interlocks, if any, and structural material providing linkage between the image receptor and diagnostic source assembly.

  • 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;

  • Collaborative pharmacy practice agreement means a written and signed

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

  • Marijuana product means marijuana as defined in 50-32-101 and marijuana-infused products

  • Marijuana products means concentrated marijuana products and marijuana products that are comprised of marijuana and other ingredients and are intended for use or consumption, such as, but not limited to, edible products, ointments, and tinctures.

  • 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.

  • Active Pharmaceutical Ingredient or “API” means the active pharmaceutical substance of the Drug in bulk form prior to incorporation into the Product.

  • Manufacturing Know-How means, with respect to the Product or any Variant thereof, the technology, data, designs, processes, methods, specifications and other know-how used in connection with the formulation, manufacture, labeling, packaging, quality control, release testing, and production of the Product, and all ingredients used therein and portions thereof.

  • Bulk drug substance means any substance that is represented for use, and that, when used in the

  • Reagent means any product other than fuel that is stored on-board the vehicle and is provided to the exhaust after-treatment system upon request of the emission control system.

  • Collaborative pharmacy practice means a practice of pharmacy whereby one or

  • Vaccine means a specially prepared antigen which, upon administration to a person, will result in immunity and, specifically for the purposes of this rule, shall mean influenza and pneumococcal vaccines.

  • Bioassay means the determination of kinds, quantities or concentrations and, in some cases, the locations of radioactive material in the human body, whether by direct measurement, in vivo counting, or by analysis and evaluation of materials excreted or removed from the human body. For purposes of these rules, “radiobioassay” is an equivalent term.

  • Antipsychotic medications means that class of drugs

  • Therapeutic diet means meals served that are soft, low-fat, low-sodium or controlled calorie.

  • Tobacco product manufacturer means an entity that after the date of enactment of this Act directly (and not exclusively through any affiliate):

  • Biological agent shall mean any pathogenic (disease producing) micro-organism(s) and/or biologically produced toxin(s) (including genetically modified organisms and chemically synthesized toxins) which cause illness and/or death in humans, animals or plants.

  • Assay means a laboratory analysis of Crude Petroleum to include the following: A.P.I. Gravity, Reid vapor pressure, composition, pour point, water and sediment content, sulfur content, viscosity, distillation, hydrogen sulfide, flash/boiling point and other characteristics as may be required by Carrier.

  • 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.

  • Drug Substance means an active ingredient that is intended to furnish pharmacological activity or other direct effect in the diagnosis, cure, mitigation, treatment, or prevention of disease or to affect the structure or any function of the human body, but does not include intermediates used in the synthesis of such ingredient.

  • Diagnostic mammography means a method of screening that

  • 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.

  • Marijuana-infused products means products that contain marijuana or marijuana extracts and are intended for human use. The term "marijuana-infused products" does not include useable marijuana.