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Minoxidil 5% (For Men)

NDC 51672-2128, Minoxidil, aerosol, foam, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-2128
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
AEROSOL, FOAM
Route
TOPICAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA209074
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-2128 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MINOXIDIL50 mg/g

Pharmacologic classes

Arteriolar Vasodilation [PE]; Arteriolar Vasodilator [EPC]

Package NDCNDC-11Package
51672-2128-4516722128041 CAN in 1 PACKAGE (51672-2128-4) / 60 g in 1 CAN
51672-2128-9516722128093 CAN in 1 PACKAGE (51672-2128-9) / 60 g in 1 CAN

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • NADAC price for package 51672212804

    GET /v1/drugs/nadac/51672212804

Use it

Look up 51672-2128 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-2128 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-2128. 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.