NDC codes

FDA NDC Directory
Product NDC (as listed)82983-403Labeler and product segments. Claims need a package NDC.
Product NDC at billing width82983-0403Add 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
82983-403-108298304031082983040310100 POUCH in 1 CARTON (82983-403-10) / 1.58 g in 1 POUCH (82983-403-01)Marketed from Mar 1, 2023
82983-403-30829830403308298304033030 POUCH in 1 CARTON (82983-403-30) / 1.58 g in 1 POUCH (82983-403-01)Marketed from Mar 1, 2023

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 for Oral Solution
Generic name (nonproprietary)
potassium chloride for oral solution
Active ingredients
Potassium chloride — 1.5 g/1.58g
Dosage form
Powder, For solution
Route
Oral
Labeler
Ajenat Pharmaceuticals LLCNDC labeler code 82983
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 212183
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 82983-403_4d98ee0a-c312-4ffd-b004-00157a4661e9SPL ID 4d98ee0a-c312-4ffd-b004-00157a4661e9SPL set ID c62c5704-3667-4d4f-8230-3f7f5ed825b1RxCUI 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

N482983040310 followed by a unit qualifier and the quantity

Package 82983-0403-10. 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)

About NDC 82983-403

What is NDC 82983-403?
82983-403 is the product NDC for Potassium Chloride for Oral Solution, Potassium chloride 1.5 g/1.58g powder, for solution, listed with the FDA by Ajenat Pharmaceuticals LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Potassium Chloride for Oral Solution.
What is the active ingredient?
Potassium chloride.
Who is the labeler?
Ajenat Pharmaceuticals LLC, NDC labeler code 82983. 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 for Oral Solution?
6 other product NDCs are listed under this name. See all Potassium Chloride for Oral Solution 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 for Oral Solution NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Potassium Chloride for Oral SolutionPotassium chloride 1.5 g/1.58gPowder, For solutionOralMarlex Pharmaceuticals, Inc.10135-80710135-0807-1310135-0807-15
Potassium Chloride for Oral SolutionPotassium chloride 1.5 g/1.58gSolutionOralMarlex Pharmaceuticals Inc10135-81910135-0819-08
Potassium Chloride for Oral SolutionPotassium chloride 3 g/4.75gSolutionOralMarlex Pharmaceuticals Inc10135-82010135-0820-08
Potassium Chloride for Oral Solutionpotassium chloridePotassium chloride 1.5 g/1.58gFor solutionOralSomerset Therapeutics, LLC70069-82370069-0823-0170069-0823-1070069-0823-30
Potassium Chloride for Oral Solutionpotassium chloridePotassium chloride 1.5 g/1.58gFor solutionOralGranules Pharmaceuticals Inc.70010-07170010-0071-4170010-0071-4270010-0071-43
Potassium Chloride for Oral SolutionPotassium chloride 1.5 g/1.58gPowder, For solutionOralBPI Labs LLC54288-12554288-0125-1054288-0125-30

Other NDCs under ANDA 212183

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

FDA NDC Directory listings under ANDA 212183
ProductStrengthForm · routeLabelerProduct NDC
Potassium Chloride for Oral SolutionPotassium chloride 1.5 g/1.58gPowder, For solutionOralMarlex Pharmaceuticals, Inc.10135-807
Potassium Chloride for Oral SolutionPotassium chloride 1.5 g/1.58gSolutionOralMarlex Pharmaceuticals Inc10135-819
Potassium Chloride for Oral SolutionPotassium chloride 3 g/4.75gSolutionOralMarlex Pharmaceuticals Inc10135-820
Potassium Chloride for Oral SolutionPotassium chloride 1.5 g/1.58gPowder, For solutionOralBPI Labs LLC54288-125

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