What is NDC 17856-0024?

17856-0024 is the product NDC for Sodium Polystyrene Sulfonate, Sodium polystyrene sulfonate 4.1 meq/g powder, for suspension, listed with the FDA by ATLANTIC BIOLOGICALS CORP.. It has 2 package NDCs, shown above in 10- and 11-digit form.

ATLANTIC BIOLOGICALS CORP., NDC labeler code 17856. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Sodium Polystyrene Sulfonate?

14 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Sodium Polystyrene Sulfonate NDC 17856-0024

NDC codes

FDA NDC Directory

Product NDC (as listed)17856-0024Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17856-0024Add 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
17856-0024-1	1785600240117856002401	50 CUP in 1 BOX, UNIT-DOSE (17856-0024-1) / 15 g in 1 CUPMarketed from Apr 11, 2023
17856-0024-2	1785600240217856002402	50 CUP in 1 BOX, UNIT-DOSE (17856-0024-2) / 30 g in 1 CUPMarketed from Apr 11, 2023

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): Sodium Polystyrene Sulfonate
Generic name (nonproprietary): sodium polystyrene sulfonate
Active ingredients: Sodium polystyrene sulfonate — 4.1 meq/g
Dosage form: Powder, For suspension
Route: Oral
Labeler: ATLANTIC BIOLOGICALS CORP.NDC labeler code 17856
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 202333
Marketing start: Apr 14, 2014
Listing expires: Dec 31, 2026
Identifiers: Product ID 17856-0024_361f79e5-0981-c4de-e063-6394a90a39acSPL ID 361f79e5-0981-c4de-e063-6394a90a39acSPL set ID 2d95d23e-94c8-4975-99f5-ce746dfbb60eRxCUI 2101899UNII 1699G8679Z

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

N417856002401 followed by a unit qualifier and the quantity

Package 17856-0024-01. 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 May 27, 2025.

Indications (excerpt from the label)

Sodium Polystyrene Sulfonate Powder, for Suspension is indicated for the treatment of hyperkalemia. Limitation of Use: Sodium Polystyrene Sulfonate Powder, for Suspension should not be used as an emergency treatment for life-threatening hyperkalemia because of its delayed onset of action [see Clinical Pharmacology (12.2)] . Sodium Polystyrene Sulfonate Powder, for Suspension is indicated for the treatment of hyperkalemia (1) . Limitation of Use: Sodium Polystyrene Sulfonate Powder, for Suspension should not be used as an emergency treatment for life-threatening hyperkalemia because of its delayed onset of action (1) .

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 17856-0024

What is NDC 17856-0024?: 17856-0024 is the product NDC for Sodium Polystyrene Sulfonate, Sodium polystyrene sulfonate 4.1 meq/g powder, for suspension, listed with the FDA by ATLANTIC BIOLOGICALS CORP.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Sodium Polystyrene Sulfonate.
What is the active ingredient?: Sodium polystyrene sulfonate.
Who is the labeler?: ATLANTIC BIOLOGICALS CORP., NDC labeler code 17856. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Sodium Polystyrene Sulfonate?: 14 other product NDCs are listed under this name. See all Sodium Polystyrene Sulfonate 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 Sodium Polystyrene Sulfonate NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Sodium Polystyrene Sulfonate	Sodium polystyrene sulfonate 15 g/60mL	SuspensionOral, Rectal	Burel Pharmaceuticals, LLC	35573-108	35573-0108-1435573-0108-57
Sodium Polystyrene Sulfonate	Sodium polystyrene sulfonate 4.1 meq/g	Powder, For suspensionOral, Rectal	SUNRISE PHARMACEUTICAL, INC.	11534-166	11534-0166-1511534-0166-1611534-0166-44
Sodium Polystyrene Sulfonate	Sodium polystyrene sulfonate 4.1 meq/g	Powder, For suspensionOral, Rectal	Bryant Ranch Prepack	63629-2390	63629-2390-01
Sodium Polystyrene Sulfonate	Sodium polystyrene sulfonate 4.1 meq/g	Powder, For suspensionOral, Rectal	Bryant Ranch Prepack	63629-8849	63629-8849-01
Sodium Polystyrene Sulfonate	Sodium polystyrene sulfonate 4.1 meq/g	Powder, For suspensionOral, Rectal	Bryant Ranch Prepack	63629-8850	63629-8850-01
Sodium Polystyrene Sulfonate	Sodium polystyrene sulfonate 4.1 meq/g	Powder, For suspensionOral, Rectal	Bryant Ranch Prepack	71335-2855	71335-2855-01
Sodium Polystyrene Sulfonate	Sodium polystyrene sulfonate 4.1 meq/g	Powder, For suspensionOral, Rectal	Bryant Ranch Prepack	72162-1230	72162-1230-0272162-1230-07
Sodium Polystyrene Sulfonate	Sodium polystyrene sulfonate 4.1 meq/g	Powder, For suspensionOral	PuraCap Laboratories, LLC	24658-760	24658-0760-16
Sodium Polystyrene Sulfonate	Sodium polystyrene sulfonate 4.1 meq/g	Powder, For suspensionOral, Rectal	Chartwell RX, LLC	62135-340	62135-0340-1162135-0340-5362135-0340-62
Sodium Polystyrene Sulfonate	Sodium polystyrene sulfonate 4.1 meq/g	Powder, For suspensionOral	Epic Pharma, LLC	42806-013	42806-0013-9442806-0013-96

All 15 Sodium Polystyrene Sulfonate NDCs

Other NDCs under ANDA 202333

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

FDA NDC Directory listings under ANDA 202333
Product	Strength	Form · route	Labeler	Product NDC
Sodium Polystyrene Sulfonate	Sodium polystyrene sulfonate 4.1 meq/g	Powder, For suspensionOral	PuraCap Laboratories, LLC	24658-760
Sodium Polystyrene Sulfonate	Sodium polystyrene sulfonate 4.1 meq/g	Powder, For suspensionOral	Epic Pharma, LLC	42806-013