Adulterated drug definition

Adulterated drug means any drug:
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Adulterated drug means a drug product which bears or contains non-nutritive sweeteners;
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Adulterated drug means a drug which contains wholly or partly, a deteriorated drug, other drugs or substances;
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Examples of Adulterated drug in a sentence

  • Adulterated drug -- Has the meaning specified in the Texas Food, Drug, and Cosmetic Act, Health and Safety Code, Chapter 431, §431.111.

  • Whereas Falsified products include Spurious drug (as defined in Section 3 (zb) of the Drugs Act 1976), Adulterated drug (as defined in Section 3 (a) of the Drugs Act 1976), Misbranded drug (as defined in Section 3 (s) of the Drugs Act 1976) and Counterfeit drug (as defined in Section 3 (f) of the Drugs Act 1976).

  • Adulterated drug tests may be considered positive test results.‌‌CLINICAL ROTATIONS AND FACILITIES‌ Please be aware that clinical rotation may require you to travel to sites as far away as Walsenburg, Lamar, Trinidad, Pueblo, Eads, or you could be as close as the hospital in La Junta.

  • Thus second phase is very suitable for them to join the network.A successful combination of the first phase cooperation networks to second phase company networks can enable a network to achieve critical mass to begin community based network model e.g. OpenSpark.

  • Division 2 Drugs etc.‌‌ 104 Adulterated drug not to be sold‌‌No person shall sell any drug or article which is adulterated or falsely described, or which is packed or enclosed for sale or labelled, branded, or marked in any manner contrary to or not in compliance with this Act.

  • Adulterated drug or medical device--as defined in § 501 of the Federal Food, Drug and Cosmetic Act, (Pub.


More Definitions of Adulterated drug

Adulterated drug means a A dangerous drug is adulterated if that is beyond the expiration date as stated by the manufacturer, packer, or distributor in its labeling or if it is not stored or dispensed according to the requirement of the federal act as indicated in the product labeling. This does not apply to expired drugs that are donated pursuant to sections 3715.88 to 3715.92 of the Revised Code. A compounded dangerous drug is considered adulterated if it exceeds:
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Adulterated drug means drug: -
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Adulterated drug means drugs:-
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Adulterated drug means any drug which differs in composition, by reason either of the addition of foreign matter or of the abstraction of any matter, from the drug ordinarily known under the same name as that which the said drug is represented to be, or which differs from the standard (if any) of such drug fixed by regulation under this Act;
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Adulterated drug means a dangerous drug that is beyond the expiration date as stated by the manufacturer, packer, or distributor in its labeling or if it is not stored or dispensed according to the requirement of the federal act as indicated in the product labeling. This does not apply to expired drugs that are donated pursuant to
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Adulterated drug means a drug that:
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Related to Adulterated drug

  • Adulterated means food or milk to which any of the following apply:

  • Misbranded means food to which any of the following apply:

  • Adulterant means any poisonous or deleterious substance in a quantity that may

  • Adulterated Specimen means a specimen that contains a substance that is not expected to be present in oral fluid, or contains a substance expected to be present but is at a concentration so high that it is not consistent with oral fluid.

  • Dangerous drug means any of the following:

  • 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).

  • Drug addiction means a disease characterized by a

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

  • Covered drug means any prescription drug that:

  • Legend drugs means any drugs which are required by state

  • controlled drug means an article or substance prescribed under a regulation to be a controlled drug.

  • Active Pharmaceutical Ingredient or “API” shall mean one or more of the following active pharmaceutical ingredients: tenofovir alafenamide (“TAF”), tenofovir disoproxil fumarate (“TDF”), elvitegravir (“EVG”), and cobicistat (“COBI”).

  • 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:

  • Biological Samples means any physical samples obtained from Study Participants in accordance with the Protocol for the purposes of the Study.

  • Chemical dependency means the physiological and psychological addiction to a controlled drug or substance, or to alcohol. Dependence upon tobacco, nicotine, caffeine or eating disorders are not included in this definition.

  • Narcotic drug means any of the following, whether produced directly or indirectly by extraction from substances of vegetable origin, or independently by means of chemical synthesis, or by a combination of extraction and chemical synthesis:

  • Biological safety cabinet means a containment unit suitable for the preparation of low to moderate risk agents where there is a need for protection of the product, personnel, and environment, according to National Sanitation Foundation (NSF) Standard 49.

  • cGMPs means current good manufacturing practices as described in Parts 210 and 211 of Title 21 of the United States’ Code of Federal Regulations, together with the latest FDA guidance documents pertaining to manufacturing and quality control practice, all as updated, amended and revised from time to time;

  • FD&C Act means the U.S. Federal Food, Drug and Cosmetic Act, as amended, and the regulations promulgated thereunder.

  • Invalid Drug Test means the result of a drug test for an oral fluid specimen that contains an unidentified adulterant, or an unidentified substance, that has abnormal physical characteristics, or that has an endogenous substance at an abnormal concentration preventing the laboratory from completing or obtaining a valid drug test result.

  • 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.

  • New drug means: (i) any drug, except a new animal drug or an animal feed bearing or containing

  • cGMP means current Good Manufacturing Practice as set forth in the United States Federal Food, Drug, and Cosmetic Act, as amended, and includes all rules and regulations promulgated by the FDA thereunder.

  • Controlled dangerous substance means a drug, substance, or

  • Anti-Static Product means a product that is labeled to eliminate, prevent, or inhibit the accumulation of static electricity. “Anti-Static Product” does not include “Electronic Cleaner,” “Floor Polish or Wax,” “Floor Coating,” and products that meet the definition of “Aerosol Coating Product” or “Architectural Coating.”

  • Prescription drug order means a lawful order of a practitioner for a drug or device for a specific patient that is communicated to a pharmacist.