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

  • Řadový zaměstnanci se zde získávají na základě smluv, které má podnik s náborovými agen- turami.

  • 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.

  • 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.

  • It has been installed in all operation rooms including sleep lab.8) Miracle Hand, the device to take filter of dialysis liquid core.9) Drug label with other languages, this service has been provided to Myanmar, Cambodian and Chinese patients of OPD and IPD.10) Red Blood Cells Rescue Can, it will help adjust the time to keep blood stable from 30 minutes to 8 hours in order to reduce the loss of blood.

  • This is how a generalization of procedures for extending collective bargaining – transforming collective agreements into “laws” so that the provisions of such agreements may be applicable to all, including those who have not signed them – would give collective bargaining a completely different dimension than in the present context.

  • Service Agreement for a Clinical Study Conduct 16/38 Preparation of the documentation for Ethics Committees X X VBL to provide: - Investigator’s Brochure - IMPD - CRF - Insurance certificate - Patient rated scales/diaries - Certificate of analysis - Drug label - Manufacturing authorisation - GMP certificate KCR to provide VBL with country specific requirements regarding submission and to prepare submission package.

  • Drug label must mention about its usage i.e. whether for internal or external use or a sample for a physician.

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

  • In addition, the free Drug is only available to patients who have been prescribed the Drug in accordance with the Drug label for an FDA-approved indication.

  • Drug label: CSS recommends the following changes to the Sponsor’s label where additions are indicated in bold underlined text and deletions have been stricken through.


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 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 printed labeling (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

  • API means the American Petroleum Institute.

  • 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.

  • 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 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

  • MFDA means the Mutual Fund Dealers Association of Canada;