Sucralfate
NDC 0713-0791, Sucralfate, suspension, from Cosette Pharmaceuticals, Inc..
- Product NDC
- 0713-0791
- Status
- Listed
- Labeler
- Cosette Pharmaceuticals, Inc.
- Dosage form
- SUSPENSION
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA217126
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0713-0791 \ -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 |
|---|---|---|
| 0713-0791-75 | 00713079175 | 420 mL in 1 BOTTLE (0713-0791-75) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/3054ce94-78a2-4da4-8b14-95311b412ab2NADAC price for package 00713079175
GET /v1/drugs/nadac/00713079175
Use it
Look up 0713-0791 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0713-0791 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0713-0791. 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.