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Desonide

NDC 51672-1281, Desonide, ointment, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-1281
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
OINTMENT
Route
TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA074254
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1281 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DESONIDE.5 mg/g

Pharmacologic classes

Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]

Package NDCNDC-11Package
51672-1281-1516721281011 TUBE in 1 CARTON (51672-1281-1) / 15 g in 1 TUBE
51672-1281-3516721281031 TUBE in 1 CARTON (51672-1281-3) / 60 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6cea3912-23ae-45f3-b535-6fea29c7594f

  • NADAC price for package 51672128101

    GET /v1/drugs/nadac/51672128101

  • NADAC price for package 51672128103

    GET /v1/drugs/nadac/51672128103

Use it

Look up 51672-1281 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1281 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-1281. 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.