NDC codes

FDA NDC Directory
Product NDC (as listed)82868-111Labeler and product segments. Claims need a package NDC.
Product NDC at billing width82868-0111Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
82868-111-90828680111908286801119090 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-111-90)Marketed from Jun 12, 2026

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
Potassium Chloride
Generic name (nonproprietary)
potassium chloride
Active ingredients
Potassium chloride — 750 mg/1
Dosage form
Tablet, Extended release
Route
Oral
Labeler
Northwind Health Company, LLCNDC labeler code 82868
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 218979
Marketing start
Listing expires
Other FDA classes
Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Potassium Compounds (Chemical structure)
Identifiers
Product ID 82868-111_54895aad-54c8-5082-e063-6394a90aefd3SPL ID 54895aad-54c8-5082-e063-6394a90aefd3SPL set ID 548953ac-31c5-a181-e063-6294a90a3b77RxCUI 628953UNII 660YQ98I10
Pharmacologic class
Osmotic Laxative; Potassium Salt

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N482868011190 followed by a unit qualifier and the quantity

Package 82868-0111-90. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective .

Indications (excerpt from the label)

Potassium chloride extended-release tablets are 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. Potassium chloride extended-release tablets are 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.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 82868-111

What is NDC 82868-111?
82868-111 is the product NDC for Potassium Chloride, Potassium chloride 750 mg/1 tablet, extended release, listed with the FDA by Northwind Health Company, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Potassium Chloride.
What is the active ingredient?
Potassium chloride.
Who is the labeler?
Northwind Health Company, LLC, NDC labeler code 82868. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Potassium Chloride?
216 other product NDCs are listed under this name. See all Potassium Chloride NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Potassium Chloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Potassium Chloridepotassium chloride oralPotassium chloride 1.5 g/15mLSolutionOralCardinal Health 107, LLC55154-802655154-8026-05
Potassium ChloridePotassium chloride 1.5 g/1.58gPowder, For solutionOralCardinal Health 107, LLC55154-835255154-8352-05
Potassium ChloridePotassium chloride 750 mg/1Tablet, Film coated, Extended releaseOralCoupler LLC67046-103267046-1032-03
Potassium ChloridePotassium chloride 750 mg/1Tablet, Film coated, Extended releaseOralSt. Mary's Medical Park Pharmacy60760-42360760-0423-90
Potassium ChloridePotassium chloride 20 meq/15mLSolutionOralAjenat Pharmaceuticals LLC82983-41182983-0411-47
Potassium ChloridePotassium chloride 40 meq/15mLSolutionOralAjenat Pharmaceuticals LLC82983-41282983-0412-47
Potassium ChloridePotassium chloride 20 meq/1Tablet, Extended releaseOralMajor Pharmaceuticals0904-754800904-7548-61
Potassium ChloridePotassium chloride 3 g/3.16gFor solutionOralIPG Pharmaceuticals, Inc.71085-08371085-0083-30
Potassium ChloridePotassium chloride 20 meq/15mLSolutionOralAurobindo Pharma Limited59651-95959651-0959-47
Potassium ChloridePotassium chloride 40 meq/15mLSolutionOralAurobindo Pharma Limited59651-96059651-0960-47

All 217 Potassium Chloride NDCs

Other NDCs under ANDA 218979

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 218979
ProductStrengthForm · routeLabelerProduct NDC
Klor-Conpotassium chloridePotassium chloride 600 mg/1Tablet, Film coated, Extended releaseOralUpsher-Smith Laboratories, LLC0245-0835
Klor-Conpotassium chloridePotassium chloride 750 mg/1Tablet, Film coated, Extended releaseOralUpsher-Smith Laboratories, LLC0245-0836
Potassium ChloridePotassium chloride 600 mg/1Tablet, Extended releaseOralUpsher-Smith Laboratories, LLC24979-229
Potassium ChloridePotassium chloride 750 mg/1Tablet, Extended releaseOralUpsher-Smith Laboratories, LLC24979-230
Potassium ChloridePotassium chloride 750 mg/1Tablet, Extended releaseOralAvKARE42291-487
Potassium ChloridePotassium chloride 750 mg/1Tablet, Extended releaseOralAphena Pharma Solutions - Tennessee, LLC71610-977

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