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SODIUM POLYSTYRENE SULFONATE

NDC 71335-2855, sodium polystyrene sulfonate, powder, for suspension, from Bryant Ranch Prepack.

Product NDC
71335-2855
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
POWDER, FOR SUSPENSION
Route
ORAL, RECTAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204071
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2855 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM POLYSTYRENE SULFONATE4.1 meq/g
Package NDCNDC-11Package
71335-2855-17133528550115 g in 1 BOTTLE (71335-2855-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d6016e9d-dec6-4f14-b10b-7ec1aba3964a

Use it

Look up 71335-2855 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2855 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-2855. 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.