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Regenpure Precision

NDC 71290-813, MINOXIDIL, liquid, from Salonceuticals, Inc..

Product NDC
71290-813
Status
Listed
Labeler
Salonceuticals, Inc.
Dosage form
LIQUID
Route
TOPICAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA076239
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71290-813 \
  -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
71290-813-02712900813021 BOTTLE in 1 BOX (71290-813-02) / 60 mL in 1 BOTTLE

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 71290-813 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71290-813 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71290-813. 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.