NDC codes

FDA NDC Directory
Product NDC (as listed)55154-8352Labeler and product segments. Claims need a package NDC.
Product NDC at billing width55154-8352Add 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
55154-8352-5551548352055 POUCH in 1 BAG (55154-8352-5) / 1.58 g in 1 POUCHMarketed from Aug 24, 2026

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 — 1.5 g/1.58g
Dosage form
Powder, For solution
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 214108
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 55154-8352_ea55ded1-e076-43de-ad3c-c75e7d0a4ebcSPL ID ea55ded1-e076-43de-ad3c-c75e7d0a4ebcSPL set ID ea55ded1-e076-43de-ad3c-c75e7d0a4ebcRxCUI 1867544UNII 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

N455154835205 followed by a unit qualifier and the quantity

Package 55154-8352-05. 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 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. Potassium Chloride 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 214108

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

FDA NDC Directory listings under ANDA 214108
ProductStrengthForm · routeLabelerProduct NDC
Potassium ChloridePotassium chloride 1.5 g/1.58gPowder, For solutionOralAdvagen Pharma Limited72888-024
Potassium ChloridePotassium chloride 1.5 g/1.58gPowder, For solutionOralNorthstar Rx LLC72603-407

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