Sucralfate
NDC 68788-8946, Sucralfate, tablet, from Preferred Pharmaceuticals Inc..
- Product NDC
- 68788-8946
- Status
- Listed
- Labeler
- Preferred Pharmaceuticals Inc.
- 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/68788-8946 \ -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 |
|---|---|---|
| 68788-8946-1 | 68788894601 | 100 TABLET in 1 BOTTLE (68788-8946-1) |
| 68788-8946-3 | 68788894603 | 30 TABLET in 1 BOTTLE (68788-8946-3) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/5ec71444-cc55-47bd-8abc-b3cfc3b47d8e
Use it
Look up 68788-8946 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8946 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 68788-8946. 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.