Prescription Drug Products definition

Prescription Drug Products means products intended for the prevention, cure or treatment of a disease, to which attach specific claims, and which has received approval from each country’s respective authorities to be marketed as a prescription drug, and which must be prescribed by a medical doctor.
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Examples of Prescription Drug Products in a sentence

  • The Company undertakes to develop Licensed Products in the Field, for application in the following end-user categories: • Over-The-Counter Products • Prescription Medical Food Products • Prescription Drug Products.

  • The Company undertakes to develop Licensed Products in the Field, for application in the following end-user categories: Over-The-Counter Products Prescription Medical Food Products Prescription Drug Products.

Related to Prescription Drug Products

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

  • 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;

  • 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 Product means a specific drug in dosage form from a known source of manufacture, whether

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

  • Labeling means all labels and other written, printed, or graphic matter on an article or any of its

  • 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.

  • Product means any deliverable under the Contract, which may include commodities, services, technology or software.

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

  • Tobacco product means any substance containing tobacco leaf, including but not limited to, cigarettes, cigars, pipe tobacco, hookah tobacco, snuff, chewing tobacco, dipping tobacco, bidis, blunts, clove cigarettes, or any other preparation of tobacco; and any product or formulation of matter containing biologically active amounts of nicotine that is manufactured, sold, offered for sale, or otherwise distributed with the expectation that the product or matter will be introduced into the human body by inhalation; but does not include any cessation product specifically approved by the U.S. Food and Drug Administration for use in treating nicotine or tobacco dependence.

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

  • Finished Product means a cannabis product in its final form to be sold at a retail premises.

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

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

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

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

  • Finished Products means the fully assembled and shrink-wrapped Licensed Products, each including a Game Cartridge, Game Cartridge label and Printed Materials.