Drug label definition

Drug label means the pamphlet accompanying an abortion-inducing drug which outlines the protocol tested and authorized by the federal food and drug administration and agreed upon by the drug company applying for the federal food and drug administration authorization of that drug. Also known as "final printing labeling instructions", drug label is the federal food and drug administration document that delineates how a drug is to be used according to the federal food and drug administration approval.
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Drug label means the pamphlet accompanying an abortion-inducing drug which
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Drug label or "drug's label" means the pamphlet
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Examples of Drug label in a sentence

  • Drug label directions for use and withdrawal periods must be followed.

  • Animals must be in good health and carcasses free of drug or chemical residues.b. Drug label directions for use and withdrawal periods must be followed.c. If drug or chemical residues are found in tissue of carcasses, the entire carcass may be condemned.

  • Therefore, the medication en- tity was treated as an open set, and the catch all Drug label was applied to all direct and indirect references to drugs.

  • The attributes related to the medication entity that were annotated include Prop:Frequency, Prop:Dosage, Prop:Mode, and Prop:Duration.In the illustrative example in Table 4, the entities– “diabetes medications”, “Sulfonylurea”, “Amaryl”, “glimepiride” – are annotated with the Drug label, while “1 mg”, “pill”, “everyday” are their attributes.One challenge encountered in this task was choosing a spe- cific label when other labels are equally valid.

  • PLX3397 HCl capsules will be stored at the clinical site, as indicated on the Study Drug label, i.e., room temperature (do not store above 25ºC/77ºF).

  • Drug label" means the pamphlet accompanying an abortion-inducing drug which outlines the protocol tested and authorized by the federal food and drug administration and agreed upon by the drug company applying for the federal food and drug administration authorization of that drug.

  • Positive in the in vitro human lymphocyte clastogenesis and mouse fibroblast assays and in vivo mouse micronucleus test Drug label.

  • All records and documents should be kept for the period contracted by the donor for the project funded by the donor.

  • An investigation into the effect of employee involvement practice on decision making process: A case study of Kumasi Anglican senior high school; a thesis submitted to the School of Graduate Studies, Kwame Nkrumah University of Science and Technology in partial fulfillment of the requirements for the degree of Master of Business Administration, 2012.3. Akuoko KO, Dwumah P, Ansong F.

  • The Act and COMMITTEE rules require the following: Drug label directions must be followed - including withdrawal periods.


More Definitions of Drug label

Drug label or “drug’s label” means the pamphlet
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Drug label means a pamphlet accompanying an
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Drug label or "drug's label" means the pamphlet accompanying an abortion-inducing drug which outlines the protocol tested and authorized by the U.S. Food and Drug Administration (FDA) and agreed upon by the drug company applying for FDA authorization of that drug. Also known as "final printing printed labeling instructions (FPL)" or referred to as the "FDA-approved label", it is the FDA-approved document which delineates how a drug is to be used according to the FDA approval;
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Drug label means a pamphlet accompanying an 1-42 abortion-inducing drug that:
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Drug label means the document published by the United
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Related to Drug label

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

  • Drug sample means a unit of a prescription drug that is not intended to be sold and is intended to promote the sale of the drug.

  • Product Labeling means, with respect to a Licensed Product in a country or other jurisdiction in the Territory, (a) the Regulatory Authority-approved full prescribing information for such Licensed Product for such country or other jurisdiction, including any required patient information, and (b) all labels and other written, printed, or graphic matter upon a container, wrapper, or any package insert utilized with or for such Licensed Product in such country or other jurisdiction.

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

  • Aerosol product means a pressurized spray system that dispenses product ingredients by means of a propellant contained in a product or a product's container, or by means of a mechanically induced force. “Aerosol Product” does not include “Pump Spray.”

  • API means American Petroleum Institute.

  • Drug outlet means a pharmacy, nursing home, shelter home, convalescent home, extended care facility, drug abuse treatment center, penal institution, hospital, family planning clinic, student health center, retail store, wholesaler, manufacturer, mail-order vendor or other establishment with facilities located within or out of this state that is engaged in dispensing, delivery or distribution of drugs within this state.

  • 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 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.

  • ANDA means an Abbreviated New Drug Application filed with the FDA pursuant to its rules and regulations.

  • 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.

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

  • 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.

  • Product Manufacturer means the entity that assembles the component parts to manufacture the final Product;

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

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

  • Drug store means a place whose principal business is, the

  • Hemp product means the same as that term is defined in § 3.2-4112.

  • Nicotine product means a product that contains nicotine and is not any of the following:

  • 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.

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

  • Non-Microsoft Product means any third-party-branded software, data, service, website or product, unless incorporated by Microsoft in a Product.

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

  • MFDA means the Mutual Fund Dealers Association of Canada;

  • Runtime Product means the version specific files and application program interfaces (APIs) specified in the RUNTIME.TXT file provided with SAP Crystal Reports 2008, SAP Crystal Reports for Eclipse 2.0, and SAP Crystal Reports for Visual Studio 2010.

  • New Product means the Synology-branded hardware product and Synology-branded accessories contained in the original packaging Customer bought from an authorized Synology distributor or reseller. You may see our “New Product” at Product Support Status.