Last Updated: May 10, 2026

Details for New Drug Application (NDA): 213467

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NDA 213467 describes POTASSIUM CHLORIDE, which is a drug marketed by Actavis Labs Fl Inc, Adare Pharms Inc, Amneal Pharms, Chartwell Molecular, Glenmark Pharms Ltd, Granules, Lupin Ltd, Nesher Pharms, Novel Labs Inc, Padagis Us, Ph Health, Prinston Inc, Strides Pharma, Teva, Tris Pharma Inc, Zydus Pharms, Ajenat Pharms, Amneal, Anda Repository, Epic Pharma Llc, Genus, Novitium Pharma, Rubicon Research, Abraxis Pharm, B Braun, Baxter Hlthcare, Fresenius Kabi Usa, Gd Searle Llc, Hospira, Intl Medication, Lilly, Luitpold, Miles, Nexus, Pharma Serve Ny, Watson Labs, Apotex, Ascent Pharms Inc, Aurobindo Pharma, Genus Lifesciences, Macleods Pharms Ltd, Pharm Assoc, Quagen, Sciegen Pharms, Taro, Wes Pharma Inc, Aurobindo Pharma Ltd, Breckenridge, Chartwell Rx, Copley Pharm, Guangzhou Novaken, Pharmobedient, Rising, Schering, Sigmapharm Labs Llc, Twi Pharms, Yichang Humanwell, Otsuka Icu Medcl, and Icu Medical Inc, and is included in one hundred and thirty-seven NDAs. It is available from seventy-one suppliers. There is one patent protecting this drug. 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. Five 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 213467

Tradename:	POTASSIUM CHLORIDE
Applicant:	Granules
Ingredient:	potassium chloride
Patents:	0

Suppliers and Packaging for NDA: 213467

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
POTASSIUM CHLORIDE	potassium chloride	FOR SOLUTION;ORAL	213467	ANDA	Granules Pharmaceuticals Inc.	70010-071	70010-071-41	1.58 g in 1 POUCH (70010-071-41)
POTASSIUM CHLORIDE	potassium chloride	FOR SOLUTION;ORAL	213467	ANDA	Granules Pharmaceuticals Inc.	70010-071	70010-071-42	30 POUCH in 1 CARTON (70010-071-42) / 1.58 g in 1 POUCH

Profile for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	FOR SOLUTION;ORAL			Strength	20MEQ
Approval Date:	Jan 27, 2022	TE:	AA	RLD:	No

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