Sucralfate
NDC 80425-0091, Sucralfate, tablet, from Advanced Rx of Tennessee, LLC.
- Product NDC
- 80425-0091
- Status
- Listed
- Labeler
- Advanced Rx of Tennessee, LLC
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA070848
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/80425-0091 \ -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 |
|---|---|---|
| 80425-0091-1 | 80425009101 | 30 TABLET in 1 BOTTLE (80425-0091-1) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/b39f22c8-f224-451a-e053-2995a90aaad7
Use it
Look up 80425-0091 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/80425-0091 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 80425-0091. 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.