United States · FDA National Drug Code directory

Imiquimod

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
45802-368_8a20139d-21d1-4182-b5aa-d59a05bf7600
Product NDC
45802-368
Form
CREAM
Composition / generic term
Imiquimod
Labeler
Padagis Israel Pharmaceuticals Ltd
Marketing category
ANDA
Marketing start / end (source format)
20101109
Source listing expiry
20261231

Source-listed ingredients

  • IMIQUIMOD — 12.5 mg/.25g

These values do not establish equivalence or a dose recommendation.

Packages

  • 12 PACKET in 1 CARTON (45802-368-53) / .25 g in 1 PACKET · 45802-368-53
  • 24 PACKET in 1 CARTON (45802-368-62) / .25 g in 1 PACKET · 45802-368-62

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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Imiquimod — United States | Molindra Medicines