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(Removed: "Treatment of Non-Alcoholic Fatty Liver Disease") alamon , Kramar B, Marolt TP, Poljak B, Milisav I

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Levocarnitine If you find any inaccurate information, please let us know by providing your feedback here This article is compiled based on the United States Pharmacopeia (USP) 2025 Edition Issued and maintained by the United States Pharmacopeial Convention (USP) C 7 H 15 NO 3 161 100 V S = Titrant volume consumed by the Sample (mL) V B = Titrant volume consumed by the Blank (mL) N A = actual normality of the Titrant (mEq/mL) F = equivalency factor, 161.2 mg/mEq W = Sample weight (mg) Acceptance criteria: 97.0%103.0% on the anhydrous basis 4 IMPURITIES Residue on Ignition 281: NMT 0.5% Chloride and Sulfate 221, Chloride Standard solution: 0.50 mL of 0.020 N hydrochloric acid Sample: 0.090 g of Levocarnitine Acceptance criteria: NMT 0.4% Enantiomeric Purity Buffer solution: Mix thoroughly 2000 mL of water with 5 mL of phosphoric acid, and add accurately 13.6 mL of triethylamine dropwise while stirring

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