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Eulexin

NDC 80725-143, Flutamide, capsule, from Waylis Therapeutics LLC.

Product NDC
80725-143
Status
Listed
Labeler
Waylis Therapeutics LLC
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075298
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/80725-143 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FLUTAMIDE125 mg/1

Pharmacologic classes

Androgen Receptor Antagonists [MoA]; Androgen Receptor Inhibitor [EPC]

Package NDCNDC-11Package
80725-143-18807250143181 BOTTLE, PLASTIC in 1 BOX (80725-143-18) / 180 CAPSULE in 1 BOTTLE, PLASTIC

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0a905e25-42b6-4937-a689-f01a8f22e644

Use it

Look up 80725-143 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/80725-143 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 80725-143. 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.