DailyMed label

Imiquimod

DailyMed label · Sun Pharmaceutical Industries, Inc. · version 8

Key facts

Product Imiquimod
Labeler Sun Pharmaceutical Industries, Inc.
Document type HUMAN PRESCRIPTION DRUG LABEL
Active ingredients IMIQUIMOD
Active ingredient UNIIs P1QW714R7M
Application number 205971
Route TOPICAL
NDC package codes 51672-4174-8, 51672-4174-6, 51672-4174-9
Effective date Jan 21, 2026
Set ID 51913a5a-1cab-4b9e-b2c2-e0174062df73

At a glance

  • 1–9 NDC package codes
  • 1–9 Active ingredients
  • 1–9 Manufacturing establishments listed

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About DailyMed drug labels

DailyMed publishes the structured product labeling (SPL) that companies submit to the FDA, including package NDCs, ingredients and the establishments that make each product.

Source: U.S. National Library of Medicine (NLM), DailyMed · Source date:

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