NDC codes

FDA NDC Directory
Product NDC (as listed)0245-0836Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00245-0836Add 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
0245-0836-1100245083611100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0245-0836-11)Marketed from Aug 15, 2025
0245-0836-1500245083615500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0245-0836-15)Marketed from Aug 15, 2025

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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)
Klor-Con
Generic name (nonproprietary)
potassium chloride
Active ingredients
Potassium chloride — 750 mg/1
Dosage form
Tablet, Film coated, Extended release
Route
Oral
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 0245-0836_ad0ecaea-8b55-4e39-a7ae-f7df5f206258SPL ID ad0ecaea-8b55-4e39-a7ae-f7df5f206258SPL set ID 4340c3f2-ecf8-44cd-9b69-217f543e24e2RxCUI 312529, 628953, 628958, 832718UNII 660YQ98I10UPC 0302450835110
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

N400245083611 followed by a unit qualifier and the quantity

Package 00245-0836-11. 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)

Klor-Con 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. KLOR-CON 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 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

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
Potassium ChloridePotassium chloride 600 mg/1Tablet, Extended releaseOralUpsher-Smith Laboratories, LLC24979-229
Klor-Conpotassium chloridePotassium chloride 600 mg/1Tablet, Film coated, Extended releaseOralUpsher-Smith Laboratories, LLC0245-0835
Potassium ChloridePotassium chloride 750 mg/1Tablet, Extended releaseOralAvKARE42291-487
Potassium ChloridePotassium chloride 750 mg/1Tablet, Extended releaseOralUpsher-Smith Laboratories, LLC24979-230
Potassium ChloridePotassium chloride 750 mg/1Tablet, Extended releaseOralNorthwind Health Company, LLC82868-111
Potassium ChloridePotassium chloride 750 mg/1Tablet, Extended releaseOralAphena Pharma Solutions - Tennessee, LLC71610-977

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