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Minoxidil

NDC 0591-5642, Minoxidil, tablet, from Actavis Pharma, Inc..

Product NDC
0591-5642
Status
Listed
Labeler
Actavis Pharma, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA071344
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0591-5642 \
  -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
0591-5642-0100591564201100 TABLET in 1 BOTTLE, PLASTIC (0591-5642-01)
0591-5642-0500591564205500 TABLET in 1 BOTTLE, PLASTIC (0591-5642-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ab30461c-f8c8-409d-9e24-d58ed8a34873

  • NADAC price for package 00591564201

    GET /v1/drugs/nadac/00591564201

  • NADAC price for package 00591564205

    GET /v1/drugs/nadac/00591564205

Use it

Look up 0591-5642 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0591-5642 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0591-5642. 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.