sodium polystyrene sulfonate
Generic: sodium polystyrene sulfonate
Labeler: puracap laboratories, llcDrug Facts
Product Profile
Brand Name
sodium polystyrene sulfonate
Generic Name
sodium polystyrene sulfonate
Labeler
puracap laboratories, llc
Dosage Form
POWDER, FOR SUSPENSION
Routes
Active Ingredients
sodium polystyrene sulfonate 4.1 meq/g
Manufacturer
Identifiers & Regulatory
Product NDC
24658-760
Product ID
24658-760_ae811fb8-9a78-496f-b710-663bc678f8e7
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202333
Listing Expiration
2026-12-31
Marketing Start
2016-12-15
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
24658760
Hyphenated Format
24658-760
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 4.1 meq/g
Packaging
- 453.6 g in 1 JAR (24658-760-16)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ae811fb8-9a78-496f-b710-663bc678f8e7", "openfda": {"nui": ["N0000178378", "N0000175357"], "unii": ["1699G8679Z"], "rxcui": ["2101899"], "spl_set_id": ["875d5288-db99-4440-8290-d9192bde6eee"], "pharm_class_epc": ["Potassium Binder [EPC]"], "pharm_class_moa": ["Potassium Ion Exchange Activity [MoA]"], "manufacturer_name": ["PuraCap Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "453.6 g in 1 JAR (24658-760-16)", "package_ndc": "24658-760-16", "marketing_start_date": "20161215"}], "brand_name": "Sodium Polystyrene Sulfonate", "product_id": "24658-760_ae811fb8-9a78-496f-b710-663bc678f8e7", "dosage_form": "POWDER, FOR SUSPENSION", "product_ndc": "24658-760", "generic_name": "Sodium Polystyrene Sulfonate", "labeler_name": "PuraCap Laboratories, LLC", "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": "20161215", "listing_expiration_date": "20261231"}