Search results

Jump to navigation Jump to search
  • |Term=Food and Drug Administration ...od clots from forming in the blood vessels in the leg. It is being studied to prevent blood clots in some cancer patients, including women having surgery
    924 bytes (130 words) - 05:11, 9 January 2023
  • |Term=Drug Therapy ...t definition=Drug Therapy - Treatment with substances other than food used to prevent, diagnose, treat or alleviate symptoms of a disease or abnormal con
    474 bytes (66 words) - 11:34, 11 January 2023
  • == New Drug Application (NDA) == ...ompany requesting the [[Food and Drug Administration]] (FDA) to consider a drug for marketing approval.
    2 KB (282 words) - 22:16, 11 February 2024
  • == United States Food and Drug Administration == ...tecting and promoting public health through the control and supervision of food safety, tobacco products, dietary supplements, prescription and over-the-co
    2 KB (288 words) - 23:13, 14 February 2024
  • == Food coloring == ...quids, powders, gels, and pastes. Food coloring is used both in commercial food production and in domestic cooking.
    2 KB (297 words) - 22:36, 8 February 2024
  • == Drug Interactions == ...omenon where a drug's effects are altered by the presence of another drug, food, drink, or some environmental chemical agents.
    2 KB (349 words) - 01:21, 13 February 2024
  • ...n (FDA). Clinical trials test how well INDs work and whether they are safe to use.  ...ntal drug, investigational drug, investigational drug, and investigational drug {{dictionary-stub}} [[Category:Dictionary of medicine]]
    833 bytes (131 words) - 23:54, 11 January 2023
  • == Abbreviated New Drug Application (ANDA) == ...States. The ANDA is submitted once the patent protection for the original drug has expired.
    2 KB (248 words) - 23:22, 3 February 2024
  • == Drug interaction == ...omenon where a drug's effects are altered by the presence of another drug, food, drink, or some environmental chemical agents.
    2 KB (254 words) - 22:32, 7 February 2024
  • '''Off-label use''' (/ɒfˈleɪbəl juːz/) refers to the practice of prescribing pharmaceuticals for an unapproved indication or ...ses, produced by the pharmaceutical company and approved by the [[Food and Drug Administration]] (FDA).
    2 KB (259 words) - 23:10, 8 February 2024
  • ...est submitted to the [[Food and Drug Administration]] (FDA) for permission to introduce, or deliver for introduction, a [[Biologic product]] into interst ...e permission granted by the regulatory authority, and "Application" refers to the act of putting something into operation.
    952 bytes (117 words) - 23:30, 14 February 2024
  • ...pharmacology]]. It refers to a type of [[generic drug]] that is equivalent to a brand-name product in dosage, strength, route of administration, quality, ...ates. The ANDA process was established by the [[Hatch-Waxman Act]] in 1984 to expedite the approval of generic drugs and increase their availability in t
    2 KB (278 words) - 16:16, 3 February 2024
  • |Term=biosimilar drug |Short definition=biosimilar drug - {{Pronunciation}} (BY-oh-SIH-mih-ler.
    955 bytes (148 words) - 01:23, 8 January 2023
  • == Food Additive == ...ɪtɪv/) is a substance added to food to enhance its flavor or appearance or to preserve its shelf life.
    2 KB (291 words) - 23:38, 8 February 2024
  • == Investigational New Drug (IND) == ...the [[pharmaceutical industry]] to describe a new drug substance or an old drug substance used in a new manner for which approval for marketing in the Unit
    2 KB (255 words) - 02:50, 12 February 2024
  • |Term=investigational drug |Short definition=investigational drug (in-VES-tih-GAY-shuh-nul .
    810 bytes (109 words) - 06:22, 12 January 2023
  • == Food Safety Initiative == ...d as /fu:d seɪfti ɪˈnɪʃɪətɪv/, the term originates from the English words "food", "safety", and "initiative".
    2 KB (219 words) - 22:03, 11 February 2024
  • == Food Labeling == ...nsumer protection]] that involves the communication of information about a food product through its packaging.
    2 KB (301 words) - 06:53, 13 February 2024
  • ...on. This designation is intended to direct overall attention and resources to the evaluation of such applications. ...s designed to facilitate the development, and expedite the review of drugs to treat serious conditions and fill an unmet medical need.
    2 KB (215 words) - 17:09, 9 February 2024
  • == National Drug Code == ...rugs intended for human use. The drug code is maintained by the [[Food and Drug Administration]] (FDA).
    1 KB (209 words) - 19:30, 11 February 2024

View (previous 20 | next 20) (20 | 50 | 100 | 250 | 500)