Package 17856-0024-1

Brand: sodium polystyrene sulfonate

Generic: sodium polystyrene sulfonate
NDC Package

Package Facts

Identity

Package NDC 17856-0024-1
Digits Only 1785600241
Product NDC 17856-0024
Description

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

Marketing

Marketing Status
Marketed Since 2023-04-11
Brand sodium polystyrene sulfonate
Generic sodium polystyrene sulfonate
Sample Package No

Linked Drug Pages (1)

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"}