sodium polystyrene sulfonate

Generic: sodium polystyrene sulfonate

Labeler: cmp pharma, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sodium polystyrene sulfonate
Generic Name sodium polystyrene sulfonate
Labeler cmp pharma, inc.
Dosage Form SUSPENSION
Routes
ORAL RECTAL
Active Ingredients

sodium polystyrene sulfonate 15 g/60mL

Manufacturer
CMP Pharma, Inc.

Identifiers & Regulatory

Product NDC 46287-006
Product ID 46287-006_233303fe-cee1-420f-bf82-aaeb7850b01f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA087859
Listing Expiration 2026-12-31
Marketing Start 1982-12-08

Pharmacologic Class

Established (EPC)
potassium binder [epc]
Mechanism of Action
potassium ion exchange activity [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 46287006
Hyphenated Format 46287-006

Supplemental Identifiers

RxCUI
313072
UPC
0346287006015
UNII
1699G8679Z
NUI
N0000178378 N0000175357

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name sodium polystyrene sulfonate (source: ndc)
Generic Name sodium polystyrene sulfonate (source: ndc)
Application Number ANDA087859 (source: ndc)
Routes
ORAL RECTAL
source: ndc

Resolved Composition

Strengths
  • 15 g/60mL
source: ndc
Packaging
  • 473 mL in 1 BOTTLE (46287-006-01)
  • 120 mL in 1 BOTTLE (46287-006-04)
  • 10 BOTTLE, UNIT-DOSE in 1 CARTON (46287-006-60) / 60 mL in 1 BOTTLE, UNIT-DOSE
source: ndc

Packages (3)

46287-006-01 473 mL in 1 BOTTLE (46287-006-01) 46287-006-04 120 mL in 1 BOTTLE (46287-006-04) 46287-006-60 10 BOTTLE, UNIT-DOSE in 1 CARTON (46287-006-60) / 60 mL in 1 BOTTLE, UNIT-DOSE

Ingredients (1)

sodium polystyrene sulfonate (15 g/60mL)

Linked Drug Pages (1)

Sodium Polystyrene Sulfonate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL", "RECTAL"], "spl_id": "233303fe-cee1-420f-bf82-aaeb7850b01f", "openfda": {"nui": ["N0000178378", "N0000175357"], "upc": ["0346287006015"], "unii": ["1699G8679Z"], "rxcui": ["313072"], "spl_set_id": ["12d48dcf-07bd-4b06-bd6c-7543f1be8357"], "pharm_class_epc": ["Potassium Binder [EPC]"], "pharm_class_moa": ["Potassium Ion Exchange Activity [MoA]"], "manufacturer_name": ["CMP Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (46287-006-01)", "package_ndc": "46287-006-01", "marketing_start_date": "19821208"}, {"sample": false, "description": "120 mL in 1 BOTTLE (46287-006-04)", "package_ndc": "46287-006-04", "marketing_start_date": "19870716"}, {"sample": false, "description": "10 BOTTLE, UNIT-DOSE in 1 CARTON (46287-006-60)  / 60 mL in 1 BOTTLE, UNIT-DOSE", "package_ndc": "46287-006-60", "marketing_start_date": "19851212"}], "brand_name": "Sodium Polystyrene Sulfonate", "product_id": "46287-006_233303fe-cee1-420f-bf82-aaeb7850b01f", "dosage_form": "SUSPENSION", "product_ndc": "46287-006", "generic_name": "sodium polystyrene sulfonate", "labeler_name": "CMP Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Polystyrene Sulfonate", "active_ingredients": [{"name": "SODIUM POLYSTYRENE SULFONATE", "strength": "15 g/60mL"}], "application_number": "ANDA087859", "marketing_category": "ANDA", "marketing_start_date": "19821208", "listing_expiration_date": "20261231"}