SODIUM POLYSTYRENE SULFONATE
NDC 72162-1230, sodium polystyrene sulfonate, powder, for suspension, from Bryant Ranch Prepack.
- Product NDC
- 72162-1230
- 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
curl https://api.healthcare.dev/v1/drugs/ndc/72162-1230 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SODIUM POLYSTYRENE SULFONATE4.1 meq/g
| Package NDC | NDC-11 | Package |
|---|---|---|
| 72162-1230-2 | 72162123002 | 454 g in 1 JAR (72162-1230-2) |
| 72162-1230-7 | 72162123007 | 15 g in 1 BOTTLE (72162-1230-7) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/9a50c6d4-e619-438d-8af9-bb758ea7ba7e
Use it
Look up 72162-1230 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72162-1230 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72162-1230. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.