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.
Drug label means the pamphlet accompanying an abortion-inducing drug which
Drug label or "drug's label" means the pamphlet

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
Drug label means a pamphlet accompanying an
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;
Drug label means a pamphlet accompanying an 1-42 abortion-inducing drug that:
Drug label means the document published by the United

Related to Drug label

  • API means American Petroleum Institute.

  • ANDA means an abbreviated new drug application filed with the FDA, pursuant to its rules and regulations (or any equivalent or replacement mechanism).

  • 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.

  • 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