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Imiquimod

NDC 51672-4145, Imiquimod, cream, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-4145
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
CREAM
Route
TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA200173
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4145 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • IMIQUIMOD50 mg/g

Pharmacologic classes

Increased Cytokine Activity [PE]; Increased Cytokine Production [PE]; Interferon Inducers [MoA]

Package NDCNDC-11Package
51672-4145-65167241450624 PACKET in 1 CARTON (51672-4145-6) / .25 g in 1 PACKET (51672-4145-8)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/59af8153-4cf8-4f22-9000-f239798d52d1

  • NADAC price for package 51672414506

    GET /v1/drugs/nadac/51672414506

Use it

Look up 51672-4145 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4145 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-4145. 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.