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Ferumoxytol

NDC 0781-3154, ferumoxytol, injection, from Sandoz Inc.

Product NDC
0781-3154
Status
Listed
Labeler
Sandoz Inc
Dosage form
INJECTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA206604
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0781-3154 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FERUMOXYTOL NON-STOICHIOMETRIC MAGNETITE510 mg/17mL

Pharmacologic classes

Iron [CS]; Parenteral Iron Replacement [EPC]

Package NDCNDC-11Package
0781-3154-01007813154011 VIAL, SINGLE-DOSE in 1 CARTON (0781-3154-01) / 17 mL in 1 VIAL, SINGLE-DOSE
0781-3154-950078131549510 VIAL, SINGLE-DOSE in 1 CARTON (0781-3154-95) / 17 mL in 1 VIAL, SINGLE-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/cf94c7fc-13a0-4ac9-bb85-9c38aa704d35

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=0781-3154

Use it

Look up 0781-3154 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0781-3154 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0781-3154. 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.