DOCUSATE SODIUM, EXTRA STRENGTH 250 MG
NDC 80513-100, DOCUSATE SODIUM, capsule, gelatin coated, from Advanced Rx LLC.
- Product NDC
- 80513-100
- Status
- Listed
- Labeler
- Advanced Rx LLC
- Dosage form
- CAPSULE, GELATIN COATED
- Route
- ORAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- OTC MONOGRAPH DRUG
- Application
- M007
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/80513-100 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- DOCUSATE SODIUM250 mg/1
| Package NDC | NDC-11 | Package |
|---|---|---|
| 80513-100-01 | 80513010001 | 100 CAPSULE, GELATIN COATED in 1 BOTTLE (80513-100-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.
Use it
Look up 80513-100 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/80513-100 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 80513-100. 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.