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OpusMeds Extra Strength Minoxidil

NDC 87338-983, MINOXIDIL, solution, from Opus Meds LLC.

Product NDC
87338-983
Status
Listed
Labeler
Opus Meds LLC
Dosage form
SOLUTION
Route
TOPICAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA076239
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/87338-983 \
  -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
87338-983-00873380983001 BOTTLE, DROPPER in 1 BOX (87338-983-00) / 60 mL in 1 BOTTLE, DROPPER

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 87338-983 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/87338-983 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 87338-983. 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.