Sucralfate
NDC 66689-305, Sucralfate, suspension, from VistaPharm, LLC.
- Product NDC
- 66689-305
- Status
- Listed
- Labeler
- VistaPharm, LLC
- Dosage form
- SUSPENSION
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA211884
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/66689-305 \ -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 |
|---|---|---|
| 66689-305-16 | 66689030516 | 1 BOTTLE, PLASTIC in 1 CARTON (66689-305-16) / 414 mL in 1 BOTTLE, PLASTIC |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/cbfbe146-5d42-4a55-9050-df2b5581487aNADAC price for package 66689030516
GET /v1/drugs/nadac/66689030516
Use it
Look up 66689-305 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/66689-305 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 66689-305. 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.