Sucralfate
NDC 52817-840, Sucralfate Oral, suspension, from TruPharma, LLC.
- Product NDC
- 52817-840
- Status
- Listed
- Labeler
- TruPharma, LLC
- Dosage form
- SUSPENSION
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA213549
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/52817-840 \ -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 |
|---|---|---|
| 52817-840-16 | 52817084016 | 473 mL in 1 BOTTLE (52817-840-16) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/7d441128-45d2-4bf2-817b-665784992e90NADAC price for package 52817084016
GET /v1/drugs/nadac/52817084016
Use it
Look up 52817-840 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/52817-840 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 52817-840. 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.