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Last Updated: May 11, 2021

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 206814

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NDA 206814 describes POTASSIUM CHLORIDE, which is a drug marketed by Actavis Labs Fl Inc, Adare Pharms Inc, Amneal Pharms, Anchen Pharms, Glenmark Pharms Ltd, Granules, Lannett Co Inc, Lupin Ltd, Nesher Pharms, Novel Labs Inc, Paddock Llc, Prinston Inc, Strides Pharma, Teva, Tris Pharma Inc, Zydus Pharms, Amneal, Belcher, Epic Pharma Llc, Pharma Res Software, Abraxis Pharm, Akorn, B Braun, Baxter Hlthcare, Fresenius Kabi Usa, Gd Searle Llc, Hospira, Intl Medication, Lilly, Luitpold, Miles, Pharma Serve Ny, Watson Labs, Apotex, Genus Lifesciences, Granules Pharms, Pharm Assoc, Amta, Ascent Pharms Inc, Aurobindo Pharma Ltd, Centaur Pharms Pvt, Copley Pharm, Mylan, Paddock Labs Llc, Schering, Sigmapharm Labs Llc, Vitruvias Therap, Yichang Humanwell, Icu Medical Inc, and Nexus Pharms, and is included in one hundred and twelve NDAs. It is available from sixty-five suppliers. Additional details are available on the POTASSIUM CHLORIDE profile page.

The generic ingredient in POTASSIUM CHLORIDE is calcium chloride; dextrose; potassium chloride; sodium chloride; sodium lactate. There are two hundred and eighty-two drug master file entries for this compound. Four suppliers are listed for this compound. Additional details are available on the calcium chloride; dextrose; potassium chloride; sodium chloride; sodium lactate profile page.
Summary for 206814
Tradename:POTASSIUM CHLORIDE
Applicant:Genus Lifesciences
Ingredient:potassium chloride
Patents:0
Formulation / Manufacturing:see details
Suppliers and Packaging for NDA: 206814
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
POTASSIUM CHLORIDE potassium chloride SOLUTION;ORAL 206814 NDA Par Pharmaceutical 0603-1542 0603-1542-58 473 mL in 1 BOTTLE, PLASTIC (0603-1542-58)
POTASSIUM CHLORIDE potassium chloride SOLUTION;ORAL 206814 NDA Par Pharmaceutical 0603-1543 0603-1543-58 473 mL in 1 BOTTLE, PLASTIC (0603-1543-58)

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:SOLUTION;ORALStrength20MEQ/15ML
Approval Date:Dec 22, 2014TE:AARLD:Yes

Profile for product number 002

Active Rx/OTC/Discontinued:RXDosage:SOLUTION;ORALStrength40MEQ/15ML
Approval Date:Dec 22, 2014TE:AARLD:Yes

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