Potassium Chloride NDC 69238-1458

NDC codes

FDA NDC Directory

Product NDC (as listed)69238-1458Labeler and product segments. Claims need a package NDC.

Product NDC at billing width69238-1458Add 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 NDC	11-digit (billing)	Package	Copy
69238-1458-2	69238145802	473 mL in 1 BOTTLE (69238-1458-2)Marketed from Jul 24, 2018
69238-1458-4	69238145804	10 CUP, UNIT-DOSE in 1 TRAY (69238-1458-4) / 15 mL in 1 CUP, UNIT-DOSE (69238-1458-3)Marketed from Jul 24, 2018

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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 — 3 g/15mL
Dosage form: Solution
Route: Oral
Labeler: Amneal Pharmaceuticals NY LLC
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 210041
Marketing start: Jul 24, 2018
Listing expires: Dec 31, 2027
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 69238-1458_db3a588c-7554-4b71-939b-277a6f037f25SPL ID db3a588c-7554-4b71-939b-277a6f037f25SPL set ID 590dd25c-c4cb-489a-a09b-eccbf1d37c1fRxCUI 312515, 314182UNII 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

N469238145802 followed by a unit qualifier and the quantity

Package 69238-1458-02. 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 Jul 1, 2026.

Indications (excerpt from the label)

Potassium chloride oral solution 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 are insufficient. Potassium chloride oral solution 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 are insufficient. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 210041

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

FDA NDC Directory listings under ANDA 210041
Product	Strength	Form · route	Labeler	Product NDC
Potassium Chloride	Potassium chloride 3 g/15mL	SolutionOral	ATLANTIC BIOLOGICALS CORP.	17856-1458
Potassium Chloride	Potassium chloride 1.5 g/15mL	SolutionOral	Amneal Pharmaceuticals NY LLC	69238-1459
Potassium Chloride	Potassium chloride 1.5 g/15mL	SolutionOral	AvPAK	50268-674
Potassium Chloride	Potassium chloride 3 g/15mL	SolutionOral	AvPAK	50268-675