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Sodium Polystyrene Sulfonate

NDC 17856-0024, Sodium Polystyrene Sulfonate, powder, for suspension, from ATLANTIC BIOLOGICALS CORP..

Product NDC
17856-0024
Status
Listed
Labeler
ATLANTIC BIOLOGICALS CORP.
Dosage form
POWDER, FOR SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202333
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/17856-0024 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM POLYSTYRENE SULFONATE4.1 meq/g
Package NDCNDC-11Package
17856-0024-11785600240150 CUP in 1 BOX, UNIT-DOSE (17856-0024-1) / 15 g in 1 CUP
17856-0024-21785600240250 CUP in 1 BOX, UNIT-DOSE (17856-0024-2) / 30 g in 1 CUP

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2d95d23e-94c8-4975-99f5-ce746dfbb60e

Use it

Look up 17856-0024 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/17856-0024 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 17856-0024. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.