Potassium Chloride (K-Tab)

Trade Name : K-Tab

AbbVie Inc.

TABLET, FILM COATED, EXTENDED RELEASE

Strength 1500 mg/1

POTASSIUM CHLORIDE Potassium Compounds [CS],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA]

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You can fill in a request for your medicine through the form provided. You can access the form by clicking on the ‘Get Price’ button.

Product information is meant for

Wholesalers Suppliers Exporters Doctors MOH Tender Supplies Hospitals Brand CROs Comparator Supplies Generic Cooperate Sourcing Individual Patients Indian Institutional Buyers

Disclaimer

Trade Marks displayed in compliance with provisions of: Trademark Act, 1999 u/s 30 and 30 (1) of "Fair use"

GNH India is WHO GDP and ISO 9001 2015 Certified Pharmaceutical Wholesaler/ Supplier/ Exporters/ Importer from India of Potassium Chloride (K-Tab) which is also known as K-Tab and Manufactured by AbbVie Inc.. It is available in strength of 1500 mg/1 per ml. Read more

Potassium Chloride (K-Tab) is supplied for Tenders/ Emergency imports/ Un - licensed, Specials, Orphan drug/ Name patient line/ RLD supplies/ Reference listed drugs/ Comparator Drug/ Bio-Similar/ Innovator samples For Clinical trials.  Click to know price.     Read less

Packaging and Delivery

Validated Cold Chain Shipment

We deliver your medicines through a validated cold chain shipment process. This process is used as these medicines need to manufactured, transported and stored at very specific temperatures, utilizing thermal and refrigerated packaging methods.

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We deliver your medicines through a validated cold chain shipment process. This process is used as these medicines need to manufactured, transported and stored at very specific temperatures, utilizing thermal and refrigerated packaging methods.

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About GNH

We deliver your medicines through a validated cold chain shipment process. This process is used as these medicines need to manufactured, transported and stored at very specific temperatures, utilizing thermal and refrigerated packaging methods.

We deliver your medicines through a validated cold chain shipment process. This process is used as these medicines need to manufactured, transported and stored at very specific temperatures, utilizing thermal and refrigerated packaging methods.

Read more
  • No data
  • K-TAB is 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.
  • K-TAB 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. n
  • No data
  • Monitor serum potassium and adjust dosages accordingly n
  • If serum potassium concentration is less than 2.5 mEq/L, use intravenous potassium instead of oral supplementation n
  • Take with meals and with a glass of water or other liquid. Swallow tablets whole. n
  • Treatment of hypokalemia:
  • Prevention of hypokalemia:
  • No data
  • 8 mEq (600 mg) oral tablets n
  • 10 mEq (750 mg) oral tablets n
  • 20 mEq (1500 mg) oral tablets n
  • Potassium chloride is contraindicated in patients on triamterene or amiloride.
  • Concomitant use with triamterene and amiloride , n
  • Solid oral dosage forms of potassium chloride can produce ulcerative and/or stenotic lesions of the gastrointestinal tract, particularly when the drug remains in contact with the gastrointestinal mucosa for a prolonged period of time. Consider the use of liquid potassium in patients with dysphagia, swallowing disorders, or severe gastrointestinal motility disorders.
  • If severe vomiting, abdominal pain, distention, or gastrointestinal bleeding occurs, discontinue K-TAB and consider possibility of ulceration, obstruction or perforation.
  • K-TAB should not be taken on an empty stomach because of its potential for gastric irritation .
  • Gastrointestinal Adverse Reactions: Can produce ulcerative and/or stenotic lesions of the gastrointestinal tract, particularly when in prolonged contact with the gastrointestinal mucosa. Take with meals. n
  • The following adverse reactions have been identified with use of oral potassium salts. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.
  • The most common adverse reactions to oral potassium salts are nausea, vomiting, flatulence, abdominal pain/discomfort, and diarrhea.
  • There have been reports of hyperkalemia and of upper and lower gastrointestinal conditions including obstruction, bleeding, ulceration, perforation .
  • Skin rash has been reported rarely.
  • Most common adverse reactions are nausea, vomiting, flatulence, abdominal pain/discomfort, and diarrhea n
  • To report SUSPECTED ADVERSE REACTIONS, contact AbbVie Inc. at 1-800-633-9110 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.
  • No data
  • Renin-angiotensin-aldosterone system inhibitors: Monitor for hyperkalemia n
  • Nonsteroidal anti-inflammatory drugs: Monitor for hyperkalemia n
  • No data
  • Cirrhosis: Initiate therapy at the low end of the dosing range n
  • Renal Impairment: Initiate therapy at the low end of the dosing range n
  • No data
  • K-TAB (potassium chloride extended-release tablets) is a solid oral dosage form of potassium chloride containing 600 mg, 750 mg and 1500 mg of potassium chloride, USP, equivalent to 8u00a0mEq, 10mEq and 20 mEq of potassium, respectively, in a film-coated (not enteric-coated), wax matrix tablet.
  • 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.
  • The 8 mEq and 10 mEq tablets also contain castor oil, cellulosic polymers, colloidal silicon dioxide, D&C Yellow No. 10, magnesium stearate, paraffin, polyvinyl acetate, titanium dioxide, vanillin, and vitamin E.
  • The 20 mEq tablets also contain castor oil, cellulosic polymers, colloidal silicon dioxide, magnesium stearate, paraffin, polyvinyl acetate, titanium dioxide, vanillin, and vitamin E.
  • No data
  • Carcinogenicity, mutagenicity and fertility studies in animals have not been performed. Potassium is a normal dietary constituent.
  • K-TAB (potassium chloride extended-release tablets, USP) contain 600 mg, 750 mg and 1500 mg of potassium chloride (equivalent to 8 mEq, 10 mEq and 20 mEq of potassium, respectively). K-TAB is provided as extended-release Filmtab tablets.
  • Recommended Storage
  • Store at room temperature 20u00b0 - 25u00b0C (68u00b0 - 77u00b0F) [see USP Controlled Room Temperature].
  • Filmtab - Film-sealed tablets, AbbVie Inc.
  • u00a92018 AbbVie Inc.
  • Manufactured by: AbbVie LTDBarceloneta, PR 00617 For: AbbVie Inc.North Chicago, IL 60064n 03-B636u00a0April, 2018
  • NDC 0074-7804-19
  • K-Tabn
  • (potassium chloride
  • extended-release
  • tablets, USP)
  • 10 mEq (750 mg)
  • 1000 Filmtabn
  • Tablets
  • Rx only abbvie
  • NDC 0074-3278-13
  • K-Tabn
  • (potassium chloride
  • extended-release
  • tablets, USP)
  • 10 mEq (750 mg)
  • 100 Filmtabn
  • Tablets
  • Rx only abbvie
  • NDC 0074-3023-13
  • K-Tabn
  • (potassium chloride
  • extended-release
  • tablets, USP)
  • 20 mEq (1500 mg)
  • 100 Filmtabn
  • Tablets
  • Rx only abbvie
  • NDC 0074-3058-41
  • K-Tabn
  • (potassium chloride
  • extended-release
  • tablets, USP)
  • 8 mEq (600 mg)
  • 100 Filmtabn
  • Tablets
  • Rx only abbvie

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