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Sulfasalazine

NDC 11534-200, Sulfasalazine, tablet, from Sunrise Pharmaceutical, Inc..

Product NDC
11534-200
Status
Listed
Labeler
Sunrise Pharmaceutical, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040349
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/11534-200 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SULFASALAZINE500 mg/1

Pharmacologic classes

Aminosalicylate [EPC]; Aminosalicylic Acids [CS]

Package NDCNDC-11Package
11534-200-0111534020001100 TABLET in 1 BOTTLE (11534-200-01)
11534-200-0411534020004500 TABLET in 1 BOTTLE (11534-200-04)
11534-200-0711534020007300 TABLET in 1 BOTTLE (11534-200-07)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a54b31cc-205d-43d3-a850-acf4b41fbc37

  • NADAC price for package 11534020001

    GET /v1/drugs/nadac/11534020001

  • NADAC price for package 11534020004

    GET /v1/drugs/nadac/11534020004

Use it

Look up 11534-200 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/11534-200 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 11534-200. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.