Sucralfate
NDC 67046-1469, Sucralfate, tablet, from Coupler LLC.
- Product NDC
- 67046-1469
- Status
- Listed
- Labeler
- Coupler LLC
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA215705
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/67046-1469 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SUCRALFATE1 g/1
Pharmacologic classes
Aluminum Complex [EPC]; Organometallic Compounds [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 67046-1469-3 | 67046146903 | 30 TABLET in 1 BLISTER PACK (67046-1469-3) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/2d586736-73ae-9af0-e063-6294a90ad875
Use it
Look up 67046-1469 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/67046-1469 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 67046-1469. 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.