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Minoxidil

NDC 68071-5324, Minoxidil, tablet, from NuCare Pharmaceuticals, Inc..

Product NDC
68071-5324
Status
Listed
Labeler
NuCare Pharmaceuticals, 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/68071-5324 \
  -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
68071-5324-36807153240330 TABLET in 1 BOTTLE, PLASTIC (68071-5324-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5bc9f21d-c959-89ee-e063-6294a90a0a62

Use it

Look up 68071-5324 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68071-5324 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68071-5324. 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.