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Amcinonide

NDC 51672-4060, Amcinonide, ointment, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-4060
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
OINTMENT
Route
TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076367
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4060 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • AMCINONIDE1 mg/g

Pharmacologic classes

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

Package NDCNDC-11Package
51672-4060-1516724060011 TUBE in 1 CARTON (51672-4060-1) / 15 g in 1 TUBE
51672-4060-2516724060021 TUBE in 1 CARTON (51672-4060-2) / 30 g in 1 TUBE
51672-4060-3516724060031 TUBE in 1 CARTON (51672-4060-3) / 60 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ac5c3e79-52f7-434e-92ae-24bd32b45edc

Use it

Look up 51672-4060 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4060 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-4060. 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.