Sulfasalazine
NDC 11534-201, Sulfasalazine, tablet, delayed release, from Sunrise Pharmaceutical, Inc..
- Product NDC
- 11534-201
- Status
- Listed
- Labeler
- Sunrise Pharmaceutical, Inc.
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA075339
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/11534-201 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SULFASALAZINE500 mg/1
Pharmacologic classes
Aminosalicylate [EPC]; Aminosalicylic Acids [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 11534-201-01 | 11534020101 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE (11534-201-01) |
| 11534-201-07 | 11534020107 | 300 TABLET, DELAYED RELEASE in 1 BOTTLE (11534-201-07) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/d596ac59-b643-4181-80ba-f2db1cc3459c
Use it
Look up 11534-201 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/11534-201 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 11534-201. 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.