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NDC 50419-751, nifurtimox, tablet, film coated, from Bayer HealthCare Pharmaceuticals Inc..

Product NDC
50419-751
Status
Listed
Labeler
Bayer HealthCare Pharmaceuticals Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA213464
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50419-751 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NIFURTIMOX120 mg/1
Package NDCNDC-11Package
50419-751-01504190751011 BOTTLE in 1 CARTON (50419-751-01) / 100 TABLET, FILM COATED in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/90d09714-a8b1-4696-8ada-f99dc54d0721

Use it

Look up 50419-751 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50419-751 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50419-751. 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.