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Minoxidil Topical Solution, 5%

NDC 51672-2151, Minoxidil Solution, solution, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-2151
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
SOLUTION
Route
TOPICAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA217998
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-2151 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MINOXIDIL50 mg/mL

Pharmacologic classes

Arteriolar Vasodilation [PE]; Arteriolar Vasodilator [EPC]

Package NDCNDC-11Package
51672-2151-4516722151041 BOTTLE in 1 CARTON (51672-2151-4) / 60 mL in 1 BOTTLE
51672-2151-9516722151093 BOTTLE in 1 CARTON (51672-2151-9) / 60 mL in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • NADAC price for package 51672215104

    GET /v1/drugs/nadac/51672215104

Use it

Look up 51672-2151 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-2151 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-2151. 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.