Sucralfate
NDC 68999-106, Sucralfate, suspension, from Chartwell Governmental & Specialty RX, LLC.
- Product NDC
- 68999-106
- Status
- Listed
- Labeler
- Chartwell Governmental & Specialty RX, LLC
- Dosage form
- SUSPENSION
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA211780
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/68999-106 \ -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 |
|---|---|---|
| 68999-106-24 | 68999010624 | 2 TRAY in 1 BOX (68999-106-24) / 10 CUP in 1 TRAY / 10 mL in 1 CUP (68999-106-10) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/d1dfbbf2-ea87-41ce-bcc4-bcba99328ed0
Use it
Look up 68999-106 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/68999-106 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 68999-106. 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.