sodium polystyrene sulfonate

Generic: sodium polystyrene sulfonate

Labeler: atlantic biologicals corp.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sodium polystyrene sulfonate
Generic Name sodium polystyrene sulfonate
Labeler atlantic biologicals corp.
Dosage Form POWDER, FOR SUSPENSION
Routes
ORAL
Active Ingredients

sodium polystyrene sulfonate 4.1 meq/g

Manufacturer
ATLANTIC BIOLOGICALS CORP.

Identifiers & Regulatory

Product NDC 17856-0024
Product ID 17856-0024_361f79e5-0981-c4de-e063-6394a90a39ac
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202333
Listing Expiration 2026-12-31
Marketing Start 2014-04-14

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 178560024
Hyphenated Format 17856-0024

Supplemental Identifiers

RxCUI
2101899
UNII
1699G8679Z
NUI
N0000178378 N0000175357

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 ANDA202333 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4.1 meq/g
source: ndc
Packaging
  • 50 CUP in 1 BOX, UNIT-DOSE (17856-0024-1) / 15 g in 1 CUP
  • 50 CUP in 1 BOX, UNIT-DOSE (17856-0024-2) / 30 g in 1 CUP
source: ndc

Packages (2)

17856-0024-1 50 CUP in 1 BOX, UNIT-DOSE (17856-0024-1) / 15 g in 1 CUP 17856-0024-2 50 CUP in 1 BOX, UNIT-DOSE (17856-0024-2) / 30 g in 1 CUP

Ingredients (1)

sodium polystyrene sulfonate (4.1 meq/g)

Linked Drug Pages (1)

Sodium Polystyrene Sulfonate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "361f79e5-0981-c4de-e063-6394a90a39ac", "openfda": {"nui": ["N0000178378", "N0000175357"], "unii": ["1699G8679Z"], "rxcui": ["2101899"], "spl_set_id": ["2d95d23e-94c8-4975-99f5-ce746dfbb60e"], "pharm_class_epc": ["Potassium Binder [EPC]"], "pharm_class_moa": ["Potassium Ion Exchange Activity [MoA]"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [{"sample": false, "description": "50 CUP in 1 BOX, UNIT-DOSE (17856-0024-1)  / 15 g in 1 CUP", "package_ndc": "17856-0024-1", "marketing_start_date": "20230411"}, {"sample": false, "description": "50 CUP in 1 BOX, UNIT-DOSE (17856-0024-2)  / 30 g in 1 CUP", "package_ndc": "17856-0024-2", "marketing_start_date": "20230411"}], "brand_name": "Sodium Polystyrene Sulfonate", "product_id": "17856-0024_361f79e5-0981-c4de-e063-6394a90a39ac", "dosage_form": "POWDER, FOR SUSPENSION", "product_ndc": "17856-0024", "generic_name": "Sodium Polystyrene Sulfonate", "labeler_name": "ATLANTIC BIOLOGICALS CORP.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Polystyrene Sulfonate", "active_ingredients": [{"name": "SODIUM POLYSTYRENE SULFONATE", "strength": "4.1 meq/g"}], "application_number": "ANDA202333", "marketing_category": "ANDA", "marketing_start_date": "20140414", "listing_expiration_date": "20261231"}