NATIONAL FORMULARY Meaning and
Definition
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The National Formulary (NF) is a comprehensive reference book that contains a collection of approved drug formulations and standards of quality and purity for pharmaceutical substances. It is widely recognized as a trustworthy resource for healthcare professionals, as it provides guidance on the proper utilization of medications and promotes safety and efficacy in pharmaceutical practice.
The NF serves as a compilation of monographs that describe specific drug products, including their composition, dosage forms, indications, and specifications. These monographs outline the necessary information regarding the physical and chemical properties of the medication, as well as methods of preparation, labeling requirements, and storage recommendations. Furthermore, the NF includes tests and assays to assess the identity, potency, and purity of each drug formulation, aiding in the determination of their overall quality.
One of the primary aims of the National Formulary is to ensure consistency and standardization within the healthcare industry. It plays a crucial role in supporting regulation and adherence to quality standards by providing a robust framework for pharmaceutical manufacturers, regulatory agencies, and healthcare professionals to follow. The NF is also regularly updated to incorporate new drug formulations and revised standards as scientific knowledge and technological advancements progress, thereby reflecting the most current information available in the field. Overall, the National Formulary plays a vital role in safeguarding public health through the provision of reliable and evidence-based drug information.
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• A collection of formulas, issued by the American Pharmaceutical Association, for the compounding of a number of preparations in more or less common use but not officially recognized by the U.S. Pharmacopeia.
• A book issued by the American Pharmaceutical Association, containing several hundred formulas of pharmaceutical preparations, not official in the Pharmacopeia, but in more or less general use by practitioners. It was first issued in 1887 and a third edition appeared in 1906; the latter was made a legal standard in the United States by the provision of the National Food and Drugs Act in January, 1907. Abbreviation: N.F.
A practical medical dictionary. By Stedman, Thomas Lathrop. Published 1920.
Common Misspellings for NATIONAL FORMULARY
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Etymology of NATIONAL FORMULARY
The word "National Formulary" has a straightforward etymology.
The term "national" originates from the Latin word "natio", which means "people" or "nation". It refers to something that relates to a whole nation or is characteristic of a particular country.
The word "formulary" comes from the Latin word "formula", meaning "a small pattern or mold". In English, "formulary" refers to a collection or list of prescribed medicines or medical preparations, typically approved by a professional body or an organization.
Therefore, when combined, "National Formulary" refers to a collection or list of approved medicines or medical preparations that are recognized at a national level. This term is commonly used in the field of pharmacy and medicine, indicating a compilation of standardized drug formulations and specifications.
