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Minoxidil

NDC 59726-115, Minoxidil, aerosol, foam, from P & L Development, LLC.

Product NDC
59726-115
Status
Listed
Labeler
P & L Development, LLC
Dosage form
AEROSOL, FOAM
Route
TOPICAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA208092
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59726-115 \
  -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
59726-115-605972601156060 g in 1 CAN (59726-115-60)
59726-115-65597260115652 CAN in 1 PACKAGE (59726-115-65) / 60 g in 1 CAN
59726-115-70597260115703 CAN in 1 PACKAGE (59726-115-70) / 60 g in 1 CAN

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

Use it

Look up 59726-115 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59726-115 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59726-115. 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.