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CYCLOPHOSPHAMIDE

NDC 10019-935, cyclophosphamide, injection, powder, for solution, from Baxter Healthcare Company.

Product NDC
10019-935
Status
Listed
Labeler
Baxter Healthcare Company
Dosage form
INJECTION, POWDER, FOR SOLUTION
Route
INTRAVENOUS, ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040745
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/10019-935 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CYCLOPHOSPHAMIDE500 mg/25mL
Package NDCNDC-11Package
10019-935-01100190935011 VIAL, SINGLE-DOSE in 1 CARTON (10019-935-01) / 25 mL in 1 VIAL, SINGLE-DOSE (10019-935-25)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6bae5c14-9e87-4fb6-ae9c-4d875c1ecffe

Use it

Look up 10019-935 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/10019-935 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 10019-935. 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.