sodium polystyrene sulfonate
Generic: sodium polystyrene sulfonate
Labeler: cmp pharma, inc.Drug Facts
Product Profile
Brand Name
sodium polystyrene sulfonate
Generic Name
sodium polystyrene sulfonate
Labeler
cmp pharma, inc.
Dosage Form
POWDER, FOR SUSPENSION
Routes
Active Ingredients
sodium polystyrene sulfonate 1 g/g
Manufacturer
Identifiers & Regulatory
Product NDC
46287-012
Product ID
46287-012_ad780ec6-1a7e-4838-b833-6adb6bdbdb9a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA089910
Listing Expiration
2026-12-31
Marketing Start
1989-01-19
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
46287012
Hyphenated Format
46287-012
Supplemental Identifiers
RxCUI
UPC
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
ANDA089910 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 g/g
Packaging
- 454 g in 1 JAR (46287-012-16)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL", "RECTAL"], "spl_id": "ad780ec6-1a7e-4838-b833-6adb6bdbdb9a", "openfda": {"nui": ["N0000178378", "N0000175357"], "upc": ["0346287012160"], "unii": ["1699G8679Z"], "rxcui": ["2101899"], "spl_set_id": ["2017bfbe-cda8-46f1-b4f1-9c086c3249a9"], "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": "454 g in 1 JAR (46287-012-16)", "package_ndc": "46287-012-16", "marketing_start_date": "19890119"}], "brand_name": "Sodium Polystyrene Sulfonate", "product_id": "46287-012_ad780ec6-1a7e-4838-b833-6adb6bdbdb9a", "dosage_form": "POWDER, FOR SUSPENSION", "product_ndc": "46287-012", "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": "1 g/g"}], "application_number": "ANDA089910", "marketing_category": "ANDA", "marketing_start_date": "19890119", "listing_expiration_date": "20261231"}