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  2. Pharmaceutical code - Wikipedia

    en.wikipedia.org/wiki/Pharmaceutical_code

    Ingredients: Unique Ingredient Identifier Proprietary database identifiers include those assigned by First Databank , Micromedex , MediSpan , Gold Standard Drug Database (published by Elsevier ), and Cerner Multum MediSource Lexicon; these are cross-indexed by RxNorm , which also assigns a unique identifier (RxCUI) to every combination of ...

  3. Pharmaceutical formulation - Wikipedia

    en.wikipedia.org/wiki/Pharmaceutical_formulation

    Pharmaceutical formulation, in pharmaceutics, is the process in which different chemical substances, including the active drug, are combined to produce a final medicinal product. The word formulation is often used in a way that includes dosage form .

  4. Unique Ingredient Identifier - Wikipedia

    en.wikipedia.org/wiki/Unique_Ingredient_Identifier

    The Unique Ingredient Identifier (UNII) is an alphanumeric identifier linked to a substance's molecular structure or descriptive information and is generated by the Global Substance Registration System (GSRS) of the Food and Drug Administration (FDA).

  5. The truth about the 'inactive ingredients' in your medications

    www.aol.com/lifestyle/2019-04-04-the-truth-about...

    To arrive at their findings, researchers searched a database of about 42,000 recipes for oral medications in the U.S. and found that close to 93 percent contained at least one of 38 inactive ...

  6. Polyvinylpyrrolidone - Wikipedia

    en.wikipedia.org/wiki/Polyvinylpyrrolidone

    PVP is included in the Inactive Ingredient Database for use in oral, topical, and injectable formulations. However, there have been documented cases of allergic reactions to PVP/povidone, particularly regarding subcutaneous (applied under the skin) use and situations where the PVP has come in contact with autologous serum (internal blood fluids ...

  7. WHO Drug Dictionary - Wikipedia

    en.wikipedia.org/wiki/WHO_Drug_Dictionary

    Seq1 is used to uniquely identify different variations (e.g. salts and esters), plant parts and extraction methods, thereby defining active substances or a combination of active substances. WHODrug records sharing the same Drug Rec No and Seq1 contain the same variation/plant part/extract variation of the same active moiety.

  8. Drug Master File - Wikipedia

    en.wikipedia.org/wiki/Drug_Master_File

    In the United States, DMFs are submitted to the Food and Drug Administration (FDA). The Main Objective of the DMF is to support regulatory requirements and to prove the quality, safety and efficacy of the medicinal product for obtaining an Investigational New Drug Application (IND), a New Drug Application (NDA),As an Abbreviated New Drug Application (ANDA), another DMF, or an Export Application.

  9. Animal products in pharmaceuticals - Wikipedia

    en.wikipedia.org/wiki/Animal_products_in...

    The use of animal parts in TCM have been definitively linked to the extinction of wildlife. [19] One example of this link is the pangolin trade, which has led the pangolin to be called the world's "most trafficked mammal." [20] In 2020, pangolin scales were removed from the Chinese list of ingredients approved for use in Traditional Chinese ...