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USP 39 Official Monographs / Calcium 1
USP 39 Official Monographs / Calcium 1. Acceptance criteria: NMT 10 ppm Calcium Citrate • LIMIT OF FLUORIDE [NOTE—Prepare and store all solutions in plastic containers.] Standard stock solution: 1000µg/mL of fluoride ion from USP Sodium Fluoride RS in water Standard solution: 5µg/mL of fluoride ion from Stan-dard stock solution.
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DISSOLUTION - USP-NF
www.uspnf.comRevision Bulletin 4 〈711〉 Dissolution Official February 1, 2012 flow rates of 4, 8, and 16 mL per minute. It must deliver a constant flow (±5% of the nominal flow rate); the flow pro-file is sinusoidal with a pulsation of 120±10 pulses per
Stearic Acid M - uspnf.com
www.uspnf.comStage 6 Harmonization Official May 1, 2016 Stearic 1. = molecular weight of potassium hydroxide, Stearic Acid M r 56.11 NF34 Acceptance criteria: 194–212 Portions of this monograph that are national USP text, and • C. The retention times of the major peaks of the Sample are not part of the harmonized text, are marked with solution correspond …
General Notices and Requirements - uspnf.com
www.uspnf.com4 General Notices USP 32 3.10.10. Applicability of Standards to Drug Products, Drugarticle.For general requirements relating to specific monograph Substances, and Excipients sections, see section 5, Monograph Components. The applicable USP or NF standard applies to any article mar-Because monographs may not provide standards for all relevant keted in the United States that (1) is …
Levetiracetam Tablets - uspnf.com
www.uspnf.comRevision Bulletin 2 Levetiracetam Official May 1, 2011 Sample solution: Pass a portion of the solution under test Mode: LC through a suitable filter. Dilute an aliquot with Medium to Detector: UV 200 nm obtain a concentration similar to that of the Standard Column: 4.6-mm × 25-cm; 4-µm packing L1 solution.
MONOGRAPHS (USP) - uspnf.com
www.uspnf.comProcedure—Transfer a sufficient portion of Test solution A and Test solution B to separate test tubes of colorless, transparent, neutralglass withaflatbaseandaninternaldia-
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www.uspnf.comLarge-volume injections for single-dose infusion, small-Aqueous vehicles—Aqueous vehicles must meet the require- volume injections, and pharmacy bulk packages (PBPs) arements of 〈151〉 or 〈85〉, whichever is specified in the mono-
1092 THE DISSOLUTION PROCEDURE: DEVELOPMENT AND …
www.uspnf.comBRIEFING 1092 The Dissolution Procedure: Development and Validation, USP 36 page 735. This general information chapter is proposed for revision by the …
Compendial Approvals for USP42-NF37 1S
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www.uspnf.comheadspace analysis, solid-phase microextraction, and direct injection of solution containing bulk drug substance or drug product into the gas chromatograph. zIn conclusion, gas chromatograph-based procedures will continue to dominate residual solvent testing because of its specificity for
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