Transfer 5.0 mL of the resulting solution to a 100-mL volumetric flask, add 2.0 mL of sodium chloride solution (1 in 5) and 1.0 mL of hydrochloride acid, dilute with water to volume, and mix. Procedure— Proceed as directed in the Assay under Potassium Chloride Oral Solution .
Additionally, minor editorial changes have been made to update the monograph to current USP style. The Potassium Chloride Extended-Release Capsules Revision Bulletin supersedes the currently official monograph. Should you have any questions, please contact Ren-Hwa Yeh, Ph.D., Senior Scientific Liaison (301-998-6818 or [email protected]).
= concentration of USP Glucosamine Hydrochloride RS in the Standard solution (mg/mL) C U = = concentration of Glucosamine Sulfate Potassium Chloride in the Sample solution (mg/mL) M r1 = = molecular weight of glucosamine sulfate potassium chloride, 605.52: M r2 = = twice the molecular weight of glucosamine hydrochloride, 431.26
USP has postponed indefinitely the official date of the revisions to the Identification, Loss on drying, and Limit of potassium tests under the Sodium Chloride Monograph, which are published on page 3582 of the USP 29–NF 24. This postponement applies to the official date of the changes, April 1, 2006.
Lactated Ringer's Injection, USP contains a total of 24 mmols of Potassium Chloride, USP. Each litre of 40 mmols Potassium Chloride in Lactated Ringer's Injection, USP contains a total of 44 mmols of Potassium Chloride, USP. It contains no antimicrobial agents. Composition, osmolarity, pH and ionic concentration are shown in Table 1.
Standard solution: To 1.5mL of Sulfate standard solu-Sodium Chloride is used can be met. . 2S (USP38) tion A add 1mL of Barium chloride solution. Shake, and allow to stand for 1 min. To 2.5mL of the resulting suspension add 15mL of Sulfate standard solution B Change to read: • . . ): in which Sodium Chloride is used.
Iodides—Moisten 5 g of Sodium Chloride by the dropwise addition of a freshly prepared mixture of 0.15 mL of sodium nitrite solution (1 in 10) 2, mL of 1 N sulfuric acid, 25 mL of iodide-free starch TS, and 25 mL of water. After 5 minutes, examine the substance in natural light. No blue color is ob- served.
Potassium chloride usually is the salt of choice in the treatment of potassium depletion, since the chloride ion is required to correct hypochloremia which frequently accompanies potassium deficiency and since the citrate, bicarbonate, gluconate, or another alkalinizing salt of potassium may cause hypochloremia, particularly when used in ...
Potassium Chloride Oral Solution 20%. Each tablespoon (15 mL) should be diluted with six (6) fluid ounces or more of water or other liquid. One (1) tablespoonful (15 mL) per day (after the morning meal) supplies 40 mEq of potassium chloride. One tablespoonful, twice a day, provides 80 mEq of potassium chloride.
Chemically, Potassium Chloride is K-Cl with a molecular mass of 74.55. Oral Solution 10%: Each 15 mL of solution contains 1.5 g of potassium chloride, USP and the following inactive ingredients: citric acid anhydrous, FD&C Yellow #6, berry citrus flavor, potassium sorbate, purified water and sodium saccharin.
Potassium chloride extended-release tablets, USP are an electrolyte replenisher. The chemical name of the active ingredient is potassium chloride, and the structural formula is KCl. Potassium chloride, USP occurs as a white, granular powder or as colorless crystals. It is odorless and has a saline taste.
Assay preparation 1 (where it is packaged in unit-dose containers)—Weigh and mix the contents of not less than 20 containers of Potassium Gluconate and Potassium Chloride for Oral Solution. Transfer an accurately weighed portion of the powder, equivalent to about 782 mg (20 mEq) of potassium, to a 100-mL volumetric flask, dilute with water to volume, and mix.
» Potassium Chloride for Injection Concentrate is a sterile solution of Potassium Chloride in Water for Injection. It contains not less than 95.0 percent and not more than 105.0 percent of the labeled amount of KCl.
Potassium chloride extended-release capsules, USP contain potassium chloride, a potassium salt indicated for the treatment and prophylaxis of hypokalemia with or without metabolic alkalosis, in patients for whom dietary management with potassium-rich foods or diuretic dose reduction is insufficient.
1mlof1 M hydrochloric acidis equivalent to 69.1 mg of K2CO3. STORAGE In an airtight container. 01/2008:0185 corrected 6.0 POTASSIUM CHLORIDE Kalii chloridum KCl Mr 74.6 [7447-40-7] DEFINITION Content: 99.0 per cent to 100.5 per cent of KCl (dried substance). CHARACTERS Appearance: white or almost white, crystalline powder or colourless crystals.
nominally 60 µg/mL of potassium chloride. Sample solution: Transfer 5.0 mL of the Sample stock solution to a 100-mL volumetric flask. Add 2.0 mL of sodium chloride solution (1 in 5) and 1.0 mL of hydrochloric acid, and dilute with water to volume. Instrumental conditions (See Atomic Absorption Spectroscopy á852ñ.)
Potassium Chloride Extended-Release Tablets 1 This text is not the official version of a USP–NF monograph and may not reflect the full and accurate contents of the currently official monograph. Please refer to the current edition of the USP–NF for
Potassium stock solution— Transfer 18.64 g of potassium chloride, previously dried at 105 for 2 hours and accurately weighed, to a 250-mL volumetric flask, add water to volume, and mix. Each mL of this stock solution contains 39.10 mg (1 mEq) of potassium.
K-TAB tablets are an electrolyte replenisher. The chemical name is potassium chloride, and the structural formula is KCl. Potassium chloride, USP, occurs as a white, granular powder or as colorless crystals. It is odorless and has a saline taste. Its solutions are neutral to litmus. It is freely soluble in water and insoluble in alcohol.
Each 15 mL (tablespoonful) contains potassium chloride 3.0 g (supplying 40 mEq of potassium and chloride) with alcohol 5%. The chemical name is potassium chloride, and the structural formula is KCl. Potassium chloride USP occurs as a white, granular powder or as colorless crystals. It is odorless and has a saline taste.
Potassium Chloride Extended-release Tablets, USP is a potassium salt, indicated for the treatment and prophylaxis of hypokalemia with or without metabolic alkalosis in patients for whom dietary management with potassium-rich foods or diuretic dose reduction is insufficient. (1) (1)
Potassium Chloride Extended Release Tablets, USP . DESCRIPTION. The Potassium Chloride Extended Release Tablets, USP 20 mEq product is an immediately dispersing extended release oral dosage form of potassium chloride containing 1500 mg of microencapsulated potassium chloride, USP equivalent to 20 mEq of potassium in a tablet.
Each contains 600 mg or 750 mg of Potassium Chloride equivalent to 8 mEq or 10 mEq of potassium in a wax matrix tablet. Potassium Chloride extended-release tablets are an electrolyte replenisher. The chemical name is Potassium Chloride, and the structural formula is KCl. Potassium Chloride, USP is a white, granular powder or colorless crystals.
Sodium Chloride. Limit of Potassium – Refer to <852> Atomic Absorption Spectroscopy Nitrites – Refer to <857> Ultraviolet-Visible Spectroscopy The Sodium Chloride monograph will be incorporated into and become official with the Second Supplement to USP 39–NF 34. The new general chapters <852>, <853>, <857> will not be applicable until May 1,...
Assay preparation 1 (where it is packaged in unit-dose containers)—Weigh and mix the contents of not less than 20 containers of Potassium Chloride for Oral Solution. Transfer an accurately weighed portion of the powder, equivalent to about 1.5 g of potassium chloride, to a 500-mL volumetric flask, dissolve in water, dilute with water to ...
1548190 USP Potassium chloride United States Pharmacopeia (USP) Reference Standard CAS Number 7447-40-7. Linear Formula KCl . Molecular Weight 74.55 . MDL number MFCD00011360. PubChem Substance ID 329750901
Potassium Chloride Injection Product Monograph Page 1 of 17. PRODUCT MONOGRAPH . Potassium Chloride Injection . Sterile Solution . Potassium ion (K +) 10 mEq/50mL, 20 mEq/50mL . 10 mEq/100mL, 20 mEq/100mL . 40mEq/100mL . Electrolyte Replenisher . Baxter Corporation Date of Revision: October 25, 2012
Labeling— Where Potassium Chloride is intended for use in hemodialysis, it is so labeled. Identification— A solution (1 in 20) responds to the tests for Potassium 191 and for Chloride 191 . Acidity or alkalinity— To a solution of 5.0 g in 50 mL of carbon dioxide–free water add 3 drops of phenolphthalein TS: no pink color is produced.
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