Solid dosage forms definition

Solid dosage forms means capsules or tablets intended for oral administration.
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Examples of Solid dosage forms in a sentence

  • Solid dosage forms should be wetted in a small amount of soapy water before tipping everything into the general medicines waste bin.

  • Primary and or Secondary Packaging only E.1 Liquid dosage formsE.2 Semi-solid dosage formsE.2 Solid dosage forms F.

  • Water activity testing is conducted as follows to determine the type of product for assigning the default BUD: • Solid dosage forms (i.e., tablets and capsules): No water activity testing is necessary.

  • Solid dosage forms such as vaginal tablets may overcome some of the compliance, acceptability and adherence issues associated with other MPT strategies.

  • Additionally, the Commission understands that the law in question applies evenhandedly, without regard to whether the pipeline supplies the intrastate or interstate market, further indicating that it does not burden interstate commerce.

  • Banks are using the technology to deliver their service since it saves cost, and uses as a competitive advantage to support their service with new developments, helps them to be accessible with the unbanked population through different delivery channels.

  • Solid dosage forms such as tablets are commonly procured in bulk and repackaged in developing countries in order control costs and therefore to ensure that governments are able to provide medicines to a large majority of the population.

  • Solid dosage forms to be separated from liquids and internal preparations to be separated from external preparations.

  • Solid dosage forms are substances having definite shape and volume manufactured for the administration of active and/or inert ingredients.

  • At the same time, there has been increasing concern among forestry staff and scientists that the forests of the ChNPP Exclusion Zone and the Mandatory (Unconditional) Resettlement Zone pose a significant risk to public health and staff health in the event of a catastrophic wildfire.

Related to Solid dosage forms

  • cosmetic product means any substance or mixture intended to be placed in contact with the external parts of the human body (epi­ dermis, hair system, nails, lips and external genital organs) or with the teeth and the mucous membranes of the oral cavity with a view exclusively or mainly to cleaning them, perfuming them, changing their appearance, protecting them, keeping them in good condition or correcting body odours;

  • medicinal product means any substance or combination of substances presented for treating or preventing disease in human beings or animals and any substance or combination of substances which may be administered to human beings or animals with a view to making a medical diagnosis or to restoring, correcting or modifying physiological functions in humans or in animals;

  • Final Product means a reasonably homogenous cannabis product in its final packaged form created using the same standard operating procedures and the same formulation.

  • Current Good Manufacturing Practices or “cGMP” means applicable Good Manufacturing Practices as specified in the United States Code of Federal Regulations and/or the EU Good Manufacturing Guidelines, and any successor legislation from time to time, prevailing at the time of the manufacture of the Product.

  • Therapeutic Product means a health product categorised as a therapeutic product in the First Schedule to the Act;

  • Red Hat Products means Software, Services, Subscriptions and other Red Hat branded offerings made available by Red Hat.

  • Therapeutic diet means meals served that are soft, low-fat, low-sodium or controlled calorie.

  • Inert ingredient means an ingredient which is not an active ingredient.

  • Active Pharmaceutical Ingredient or “API” shall mean one or more of the following active pharmaceutical ingredients: tenofovir alafenamide (“TAF”), tenofovir disoproxil fumarate (“TDF”), elvitegravir (“EVG”), and cobicistat (“COBI”).

  • Food and food ingredients means substances, whether in liquid, concentrated, solid, frozen, dried, or dehydrated form, that are sold for ingestion or chewing by humans and are consumed for their taste or nutritional value. Food and food ingredients do not include alcoholic beverages and tobacco.

  • Good Manufacturing Practices means current good manufacturing practices, as set forth in 21 C.F.R. Parts 210 and 211.

  • Tobacco products means cigars, cigarettes, cheroots, stogies, periques, granulated, plug cut, crimp cut, ready rubbed, and other smoking tobacco, snuff, snuff flour, moist snuff, cavendish, ping and twist tobacco, fine-cut and other chewing tobaccos, shorts, refuse scraps, clippings, cuttings and sweepings of tobacco, and other kinds and forms of tobacco, prepared in such manner as to be suitable for chewing or smoking in a pipe or otherwise, or both for chewing and smoking.

  • Finished Products means any one or more of the following petroleum oils, or a mixture or combination of these oils, to be used without further processing except blending by mechanical means:

  • Marijuana-infused products means products that contain marijuana or marijuana extracts and are intended for human use. The term "marijuana-infused products" does not include useable marijuana.

  • Therapeutic school means a residential group living facility:

  • Tobacco product means any substance containing tobacco leaf, including but not limited to, cigarettes, cigars, pipe tobacco, hookah tobacco, snuff, chewing tobacco, dipping tobacco, bidis, blunts, clove cigarettes, or any other preparation of tobacco; and any product or formulation of matter containing biologically active amounts of nicotine that is manufactured, sold, offered for sale, or otherwise distributed with the expectation that the product or matter will be introduced into the human body by inhalation; but does not include any cessation product specifically approved by the U.S. Food and Drug Administration for use in treating nicotine or tobacco dependence.

  • Finished Product means a cannabis product in its final form to be sold at a retail premises.

  • Good Manufacturing Practice or “GMP” means the current good manufacturing practices applicable from time to time to the manufacturing of a Product or any intermediate thereof pursuant to Applicable Law.

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

  • Labeling means all labels and other written, printed, or graphic matter on an article or any of its

  • Radiopharmaceutical service means, but is not limited to, the procurement, storage, handling preparation, labeling, quality assurance testing, dispensing, delivery, recordkeeping, and disposal of radiopharmaceuticals and other drugs.

  • GMPs means the then-current good manufacturing practices required by the FDA, as defined in 21 C.F.R. Parts 210 and 211 and the regulations promulgated thereunder, for the manufacture and testing of pharmaceutical materials, and comparable laws or regulations applicable to the manufacture and testing of pharmaceutical materials in jurisdictions outside the U.S., as they may be updated from time to time. GMPs shall include applicable quality guidelines promulgated under the International Conference on Harmonization.

  • API means the American Petroleum Institute.

  • Licensed Products means tangible materials which, in the course of manufacture, use, sale, or importation, would be within the scope of one or more claims of the Licensed Patent Rights that have not been held unpatentable, invalid or unenforceable by an unappealed or unappealable judgment of a court of competent jurisdiction.

  • Licensed Services means all functions performed by the Licensed System.

  • Marijuana products means concentrated marijuana products and marijuana products that are comprised of marijuana and other ingredients and are intended for use or consumption, such as, but not limited to, edible products, ointments, and tinctures.