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MINOXIDIL

NDC 53489-386, minoxidil, tablet, from Sun Pharmaceutical Industries, Inc..

Product NDC
53489-386
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA072709
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/53489-386 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MINOXIDIL2.5 mg/1

Pharmacologic classes

Arteriolar Vasodilation [PE]; Arteriolar Vasodilator [EPC]

Package NDCNDC-11Package
53489-386-0153489038601100 TABLET in 1 BOTTLE (53489-386-01)
53489-386-0353489038603250 TABLET in 1 BOTTLE (53489-386-03)
53489-386-0553489038605500 TABLET in 1 BOTTLE (53489-386-05)
53489-386-10534890386101000 TABLET in 1 BOTTLE (53489-386-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0354a7f5-5917-44dc-9963-411104008cb5

  • NADAC price for package 53489038601

    GET /v1/drugs/nadac/53489038601

Use it

Look up 53489-386 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/53489-386 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 53489-386. 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.