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Imiquimod

NDC 0093-3133, imiquimod, cream, from Teva Pharmaceuticals USA, Inc..

Product NDC
0093-3133
Status
Listed
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
CREAM
Route
TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA022483
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0093-3133 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • IMIQUIMOD37.5 mg/g

Pharmacologic classes

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

Package NDCNDC-11Package
0093-3133-31000933133311 BOTTLE, PUMP in 1 CARTON (0093-3133-31) / 7.5 g in 1 BOTTLE, PUMP

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9f2cbefd-f295-47e2-8a9e-3e7c5812c963

  • NADAC price for package 00093313331

    GET /v1/drugs/nadac/00093313331

Use it

Look up 0093-3133 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0093-3133 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0093-3133. 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.