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Sodium Polystyrene Sulfonate

NDC 10702-036, Sodium Polystyrene Sulfonate, powder, from KVK-Tech, Inc..

Product NDC
10702-036
Status
Listed
Labeler
KVK-Tech, Inc.
Dosage form
POWDER
Route
ORAL, RECTAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040905
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/10702-036 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM POLYSTYRENE SULFONATE1 g/g
Package NDCNDC-11Package
10702-036-151070200361515 g in 1 BOTTLE (10702-036-15)
10702-036-4510702003645454 g in 1 JAR (10702-036-45)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/905c3ee5-d1a7-4deb-a345-4a42296704fa

  • NADAC price for package 10702003615

    GET /v1/drugs/nadac/10702003615

  • NADAC price for package 10702003645

    GET /v1/drugs/nadac/10702003645

Use it

Look up 10702-036 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/10702-036 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 10702-036. 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.