Sucralfate
NDC 54738-005, Sucralfate, suspension, from Richmond Pharmaceuticals, Inc..
- Product NDC
- 54738-005
- Status
- Listed
- Labeler
- Richmond Pharmaceuticals, Inc.
- Dosage form
- SUSPENSION
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA216726
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/54738-005 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SUCRALFATE1 g/10mL
Pharmacologic classes
Aluminum Complex [EPC]; Organometallic Compounds [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 54738-005-42 | 54738000542 | 420 mL in 1 BOTTLE (54738-005-42) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/7ac10c3f-9d50-4702-900c-41075ac6f896
Use it
Look up 54738-005 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/54738-005 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 54738-005. 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.