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Sulfasalazine

NDC 70518-1829, Sulfasalazine, tablet, from REMEDYREPACK INC..

Product NDC
70518-1829
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA007073
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-1829 \
  -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
70518-1829-37051818290330 TABLET in 1 BLISTER PACK (70518-1829-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/88441a9f-b4f9-455d-a355-46fb30699a7b

Use it

Look up 70518-1829 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-1829 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-1829. 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.