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NDC 59137-335, treosulfan, injection, powder, lyophilized, for solution, from Medexus Pharma, Inc..

Product NDC
59137-335
Status
Listed
Labeler
Medexus Pharma, Inc.
Dosage form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA214759
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59137-335 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TREOSULFAN1000 mg/g
Package NDCNDC-11Package
59137-335-01591370335011 VIAL in 1 CARTON (59137-335-01) / 1 g in 1 VIAL

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2d06b03c-17aa-0492-e063-6294a90abd8f

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=59137-335

Use it

Look up 59137-335 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59137-335 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59137-335. 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.