Prescription drug · ANDA

Sodium Polystyrene Sulfonate NDC 46287-006

Sodium polystyrene sulfonate 15 g/60mL · Suspension · Oral, Rectal · CMP Pharma, Inc.

NDC codes

FDA NDC Directory
Product NDC (as listed)46287-006Labeler and product segments. Claims need a package NDC.
Product NDC at billing width46287-0006Add 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
46287-006-014628700060146287000601473 mL in 1 BOTTLE (46287-006-01)Marketed from Dec 8, 1982
46287-006-044628700060446287000604120 mL in 1 BOTTLE (46287-006-04)Marketed from Jul 16, 1987
46287-006-60462870006604628700066010 BOTTLE, UNIT-DOSE in 1 CARTON (46287-006-60) / 60 mL in 1 BOTTLE, UNIT-DOSEMarketed from Dec 12, 1985

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)
Sodium Polystyrene Sulfonate
Generic name (nonproprietary)
sodium polystyrene sulfonate
Active ingredients
Sodium polystyrene sulfonate — 15 g/60mL
Dosage form
Suspension
Route
Oral, Rectal
Labeler
CMP Pharma, Inc.NDC labeler code 46287
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 087859
Marketing start
Listing expires
Identifiers
Product ID 46287-006_233303fe-cee1-420f-bf82-aaeb7850b01fSPL ID 233303fe-cee1-420f-bf82-aaeb7850b01fSPL set ID 12d48dcf-07bd-4b06-bd6c-7543f1be8357RxCUI 313072UNII 1699G8679ZUPC 0346287006015

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N446287000601 followed by a unit qualifier and the quantity

Package 46287-0006-01. 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 .

Indications (excerpt from the label)

INDICATION AND USAGE SPS ® Suspension is indicated for the treatment of hyperkalemia.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 46287-006

What is NDC 46287-006?
46287-006 is the product NDC for Sodium Polystyrene Sulfonate, Sodium polystyrene sulfonate 15 g/60mL suspension, listed with the FDA by CMP Pharma, Inc.. It has 3 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?
CMP Pharma, Inc., NDC labeler code 46287. 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Sodium Polystyrene SulfonateSodium polystyrene sulfonate 15 g/60mLSuspensionOral, RectalBurel Pharmaceuticals, LLC35573-10835573-0108-1435573-0108-57
Sodium Polystyrene SulfonateSodium polystyrene sulfonate 4.1 meq/gPowder, For suspensionOral, RectalSUNRISE PHARMACEUTICAL, INC.11534-16611534-0166-1511534-0166-1611534-0166-44
Sodium Polystyrene SulfonateSodium polystyrene sulfonate 4.1 meq/gPowder, For suspensionOral, RectalBryant Ranch Prepack63629-239063629-2390-01
Sodium Polystyrene SulfonateSodium polystyrene sulfonate 4.1 meq/gPowder, For suspensionOral, RectalBryant Ranch Prepack63629-884963629-8849-01
Sodium Polystyrene SulfonateSodium polystyrene sulfonate 4.1 meq/gPowder, For suspensionOral, RectalBryant Ranch Prepack63629-885063629-8850-01
Sodium Polystyrene SulfonateSodium polystyrene sulfonate 4.1 meq/gPowder, For suspensionOral, RectalBryant Ranch Prepack71335-285571335-2855-01
Sodium Polystyrene SulfonateSodium polystyrene sulfonate 4.1 meq/gPowder, For suspensionOral, RectalBryant Ranch Prepack72162-123072162-1230-0272162-1230-07
Sodium Polystyrene SulfonateSodium polystyrene sulfonate 4.1 meq/gPowder, For suspensionOralPuraCap Laboratories, LLC24658-76024658-0760-16
Sodium Polystyrene SulfonateSodium polystyrene sulfonate 4.1 meq/gPowder, For suspensionOral, RectalChartwell RX, LLC62135-34062135-0340-1162135-0340-5362135-0340-62
Sodium Polystyrene SulfonateSodium polystyrene sulfonate 4.1 meq/gPowder, For suspensionOralATLANTIC BIOLOGICALS CORP.17856-002417856-0024-0117856-0024-02

All 15 Sodium Polystyrene Sulfonate NDCs

Other NDCs under ANDA 087859

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

FDA NDC Directory listings under ANDA 087859
ProductStrengthForm · routeLabelerProduct NDC
Sodium Polystyrene SulfonateSodium polystyrene sulfonate 15 g/60mLSuspensionOral, RectalCardinal Health 107, LLC55154-7353

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