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Minoxidil

NDC 71335-3120, Minoxidil, tablet, from Bryant Ranch Prepack.

Product NDC
71335-3120
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA071345
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-3120 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MINOXIDIL10 mg/1

Pharmacologic classes

Arteriolar Vasodilation [PE]; Arteriolar Vasodilator [EPC]

Package NDCNDC-11Package
71335-3120-171335312001100 TABLET in 1 BOTTLE (71335-3120-1)
71335-3120-27133531200230 TABLET in 1 BOTTLE (71335-3120-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f76f6a05-11f8-48a6-98a3-b1407c228089

Use it

Look up 71335-3120 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-3120 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-3120. 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.