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  2. Modified-release dosage - Wikipedia

    en.wikipedia.org/wiki/Modified-release_dosage

    Modified-release dosage is a mechanism that (in contrast to immediate-release dosage) delivers a drug with a delay after its administration (delayed-release dosage) or for a prolonged period of time (extended-release [ER, XR, XL] dosage) or to a specific target in the body (targeted-release dosage). [1] Sustained-release dosage forms are dosage ...

  3. Category:Dosage forms - Wikipedia

    en.wikipedia.org/wiki/Category:Dosage_forms

    Self-microemulsifying drug delivery system; Sink condition; Smoking; Snuff (tobacco) Softgel; Sol–gel process; Solution (chemistry) Subcutaneous administration; Suppository; Suspension (chemistry) Modified-release dosage; Syrup

  4. Dosage form - Wikipedia

    en.wikipedia.org/wiki/Dosage_form

    Dosage forms vary depending on the method/route of administration, which can include many types of liquid, solid, and semisolid forms. Common dosage forms include tablets, capsules, drinks, and syrups, among others. A combination drug (or fixed-dose combination; FDC) is a product that contains more than one active ingredient (e.g., one tablet ...

  5. Pharmaceutical formulation - Wikipedia

    en.wikipedia.org/wiki/Pharmaceutical_formulation

    A low drug load may cause homogeneity problems. A high drug load may pose flow problems or require large capsules if the compound has a low bulk density. By the time phase III clinical trials are reached, the formulation of the drug should have been developed to be close to the preparation that will ultimately be used in the market. A knowledge ...

  6. Liberation (pharmacology) - Wikipedia

    en.wikipedia.org/wiki/Liberation_(pharmacology)

    Release (Liberation) is the first step in the process by which medication enters the body and liberates the active ingredient that has been administered. The pharmaceutical drug must separate from the vehicle or the excipient that it was mixed with during manufacture. Some authors split the process of liberation into three steps: disintegration ...

  7. Depot injection - Wikipedia

    en.wikipedia.org/wiki/Depot_injection

    Depot injections can be created by modifying the drug molecule itself, as in the case of prodrugs, or by modifying the way it is administered, as in the case of oil/lipid suspensions. Depot injections can have a duration of action of one month or greater and are available for many types of drugs, including antipsychotics and hormones .

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    mail.aol.com

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  9. IVIVC - Wikipedia

    en.wikipedia.org/wiki/IVIVC

    An in-vitro in-vivo correlation (IVIVC) has been defined by the U.S. Food and Drug Administration (FDA) as "a predictive mathematical model describing the relationship between an in-vitro property of a dosage form and an in-vivo response".