sevelamer hydrochloride
NDC 68462-446, sevelamer hydrochloride, tablet, film coated, from Glenmark Pharmaceuticals Inc., USA.
- Product NDC
- 68462-446
- Status
- Listed
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA204724
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/68462-446 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SEVELAMER HYDROCHLORIDE400 mg/1
Pharmacologic classes
Phosphate Binder [EPC]; Phosphate Chelating Activity [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 68462-446-26 | 68462044626 | 360 TABLET, FILM COATED in 1 BOTTLE (68462-446-26) |
| 68462-446-30 | 68462044630 | 30 TABLET, FILM COATED in 1 BOTTLE (68462-446-30) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/2cd6512f-0edd-4a30-a4fa-aa996038633c
Use it
Look up 68462-446 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/68462-446 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 68462-446. 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.