Pure Food and Drug Laws definition

Pure Food and Drug Laws means the FFDC Act and the pure food and drug laws of each of the states of the United States into which products of the Business, the Log Cabin Business and the Xxxxxx Xxxxx Business are or have been shipped.
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Pure Food and Drug Laws means (i) the Federal Food, Drug and Cosmetic Act, as amended from time to time, and any successor statute and (ii) the pure food and drug laws of each of the states of the United States into which products manufactured, marketed or sold by the Borrowers are or have been shipped.
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Examples of Pure Food and Drug Laws in a sentence

  • Company shall, and shall cause each of its Subsidiaries to, comply with the requirements of all applicable laws, rules, regulations and orders of any governmental authority (including all Pure Food and Drug Laws), noncompliance with which could reasonably be expected to cause a Material Adverse Effect.

  • Comply with requirements of all applicable laws, rules, regulations and orders of any Governmental Authority (including all Pure Food and Drug Laws), except to the extent that failure to comply herewith could not, in the aggregate, have a Material Adverse Effect (other than any non-compliance solely with respect to the ABA Pension Plan).

  • Comply with requirements of all applicable laws, rules, regulations and orders of any Governmental Authority (including all Pure Food and Drug Laws), except to the extent that failure to comply herewith could not, in the aggregate, have a Material Adverse Effect.

Related to Pure Food and Drug Laws

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

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

  • New Drug Application or “NDA” means a New Drug Application filed with the FDA as described in 21 C.F.R. § 314, a Biological License Application (BLA) pursuant to 21 C.F.R. § 601.2, or any equivalent or any corresponding application for Regulatory Approval (not including pricing and reimbursement approval) in any country or regulatory jurisdiction other than the United States.

  • Criminal drug statute means a Federal or non-Federal criminal statute involving the manufacture, distribution, dispensing, possession or use of any controlled substance.

  • Legend drug or "prescription drug" means any drug or device that has been determined to be unsafe for self- medication or any drug or device that bears or is required to bear the legend:

  • FFDCA means the United States Federal Food, Drug, and Cosmetic Act, 21 U.S.C. § 301 et seq., as amended from time to time, together with any rules, regulations and requirements promulgated thereunder (including all additions, supplements, extensions, and modifications thereto).

  • Legend drugs means any drugs which are required by state

  • FD&C Act means the United States Federal Food, Drug and Cosmetic Act, as amended.

  • FDA Laws means all applicable statutes (including the FDCA), rules and regulations implemented administered or enforced by the FDA (and any foreign equivalent).

  • Foreign Financial Regulatory Authority shall have the meaning given by Section 2(a)(50) of the 0000 Xxx.

  • Biologics License Application or “BLA” means, with respect to a country or extra-national territory, a request for permission to introduce, distribute, sell or market a biologic product in such country or some or all of such extra-national territory, including pursuant to 21 CFR 601.2 in the U.S.

  • Legal drug means any drug, including any prescription drug or over-the-counter drug, that has been legally obtained and that is not unlawfully sold or distributed.

  • foreign regulatory authority means a securities commission, exchange or other securities market regulatory authority in a designated foreign jurisdiction;

  • national regulatory authority means the body or bodies charged by a Member State with any of the regulatory tasks assigned in this Directive and the Specific Directives;

  • Governmental Regulations means all statutes, ordinances, rules and regulations of the Authorities applicable to Seller or the use or operation of the Real Property or the Improvements or any portion thereof.

  • MHLW means the Japanese Ministry of Health, Labor and Welfare, or a successor agency thereto.

  • FDA Act means the U.S. Federal Food, Drug, and Cosmetic Act, as amended.

  • Covered drug means any prescription drug that:

  • Health Canada means the section of the Canadian Government known as Health Canada and includes, among other departments, the Therapeutic Products Directorate and the Health Products and Food Branch Inspectorate;