SEVELAMER HYDROCHLORIDE
NDC 59651-088, SEVELAMER HYDROCHLORIDE, tablet, film coated, from Aurobindo Pharma Limited.
- Product NDC
- 59651-088
- Status
- Listed
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA212599
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/59651-088 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SEVELAMER HYDROCHLORIDE800 mg/1
Pharmacologic classes
Phosphate Binder [EPC]; Phosphate Chelating Activity [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 59651-088-18 | 59651008818 | 180 TABLET, FILM COATED in 1 BOTTLE (59651-088-18) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/d8729e42-dbbd-4954-9ce0-298743a15a06NADAC price for package 59651008818
GET /v1/drugs/nadac/59651008818
Use it
Look up 59651-088 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/59651-088 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 59651-088. 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.