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Constitute the entire contents ofvial of the RSE withmL of LAL Reagent Water 3, ANTIMICROBIAL EFFECTIVENESS TESTING. INTRODUCTION. This general information chapter provides General ChaptersIDENTIFICATION TESTS-GENERALIDENTIFICATION TESTS GENERAL. Antimicrobial preservatives are substances added to nonsterile dosage forms to protect them from microbiological Labeling— The label of each individual container (packet) of Suture indicates the size, length, type of Suture, kind of needle (if a needle is included), number of sutures (if Sulfate— Dissolve the specified quantity of the substance under test intomL of water, or, where the substance is already in solution, add water to make a total volume ofto USP, NF the United States Pharmacopeia, the National Formulary. [NOTE The tests are not intended to be applicable to mixtures of substances unless so specified.] United States Pharmacopeial Convention, USPNF USPFront Matter: USPFront Matter: NFReference Tables: Description and SolubilityAReference Tables: Description and SolubilityBReference Tables: Description and SolubilityCReference Tables: Description and SolubilityD In, the chapter became official with the Second Supplement to USP–NF(2–4). The USP Endotoxin RS has a defined potency of, USP Endotoxin Units (EU) per vial. The General Chapters—Dosage Forms Expert Committee – placed the review and possible revision of The Dissolution Procedure: Development and Validation on its work plan for the – revision cycle () (5) USP–NF USP-NF WATER FOR PHARMACEUTICAL PURPOSES. Water is widely used as a raw material, ingredient, and solvent in the processing, formulation, and manufacture of pharmaceutical products, active pharmaceutical ingredients (APIs) and intermediates, compendial articles, and analytical reagents. Under this heading are placed tests that are frequently referred to in the Pharmacopeia for the identification of official articles.
