SODIUM POLYSTYRENE SULFONATE
NDC 63629-8850, sodium polystyrene sulfonate, powder, for suspension, from Bryant Ranch Prepack.
- Product NDC
- 63629-8850
- 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/63629-8850 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SODIUM POLYSTYRENE SULFONATE4.1 meq/g
| Package NDC | NDC-11 | Package |
|---|---|---|
| 63629-8850-1 | 63629885001 | 15 g in 1 BOTTLE (63629-8850-1) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/fe1eaaea-0697-4790-8f14-b9db08d42257
Use it
Look up 63629-8850 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/63629-8850 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 63629-8850. 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.