OTC Drug definition

OTC Drug means a non-prescription drug.
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OTC Drug means a Drug with a Medi-Span Rx-OTC Indicator Code of “O” or “P.”
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OTC Drug means a drug that may be dispensed, retailed, and used without a prescription on the list of OTC drugs promulgated by the Minister of Health.
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Examples of OTC Drug in a sentence

  • Any additions to the Contractor OTC Drug Formulary are required to only be from participating rebating labelers.

  • The Contractor shall maintain an Over-the-Counter (OTC) Drug Formulary and Contraception Formularies and a Pharmacy Supplements Formulary which contains, at a minimum, the same items included in the FFS OTC Drug Formulary and Contraception Formularies and the Pharmacy Supplements Formulary and as updated by the DUR Board.

  • The Contractor shall maintain an Over-the-Counter (OTC) Drug Formulary and Pharmacy Supplements Formulary which contains, at a minimum, the same items included in the FFS OTC Drug Formulary and Pharmacy Supplements Formulary and as updated by the DUR Board.

  • An OTC drug is covered by the OTC Drug Review if its conditions of use existed in the OTC drug marketplace on or before May 11, 1972 (37 FR 9464) (Ref.

  • The Over-the-Counter (OTC) Drug List tells you how to find out which drugs are covered under MassHealth Standard (Medicaid).

  • Drugs, however, must generally either receive premarket approval by FDA through the New Drug Application (NDA) process or conform to a "monograph" for a particular drug category, as established by FDA's Over-the-Counter (OTC) Drug Review.

  • The new "OTC Drug" received FDA registration during the second quarter of 2017 (NDC:69006-010-00) and the Company's name of the new drug will portray prolonged endurance.

  • The Contractor shall maintain an Over the Counter (OTC) Drug Formulary and Contraception Formularies and a Pharmacy Supplements Formulary which contains, at a minimum, the same items included in the FFS OTC Drug Formulary and Contraception Formularies and the Pharmacy Supplements Formulary and as updated by the DUR Board.

  • Whitney, Product Liability Issues for the Expanding OTC Drug Category, 48 Food & Drug L.

  • Certain OTC Drugs, listed in the Medication Guide, may be covered when you get a Prescription for the OTC Drug from your Physician.

Related to OTC Drug

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

  • Generic Drug means a Prescription Drug that is medically equivalent to a Brand Name Drug as determined by the FDA. It meets the same standards as a Brand Name Drug for purity, safety, strength and effectiveness and is manufactured and sold under its chemical, common, or official name.

  • Covered drug means any prescription drug that:

  • 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:

  • OTC Market means any over-the-counter market or over-the-telephone market in any country in any part of the world, and in relation to any particular Authorised Investment shall be deemed to include any responsible firm, corporation or association in any country in any part of the world dealing in the Authorised Investment which the Manager may from time to time elect.

  • Automated drug dispensing system means a mechanical or electronic system that performs

  • Legend drugs means any drugs which are required by state

  • 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 Application means a new drug application in the United States for authorization to market a product, as defined in the applicable laws and regulations and submitted to the FDA.

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

  • OTC Markets means either OTC QX or OTC QB of the OTC Markets Group, Inc.

  • OTCQX means the OTCQX tier of the OTC Markets Group Inc.

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

  • OTC means Over-the-Counter.

  • 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).

  • MHLW means the Japanese Ministry of Health, Labour and Welfare, and any successor agency thereto.

  • Relevant Electric Retail Regulatory Authority means an entity that has jurisdiction over and establishes prices and policies for competition for providers of retail electric service to end- customers, such as the city council for a municipal utility, the governing board of a cooperative utility, the state public utility commission or any other such entity.

  • Over-the-counter drug means a drug that contains a label

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

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

  • Brand Name Drug means a Prescription Drug that has been given a name by a manufacturer or distributor to distinguish it as produced or sold by a specific manufacturer or distributor and may be used and protected by a trademark.

  • OTCQB means the OTCQB Market.

  • OTC Bulletin Board means the over-the-counter electronic bulletin board.

  • Prescription drug means any drug required by federal law or regulation to be dispensed only

  • 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:

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