NDCFind

Imiquimod 51672-4145-06

Package NDC

51672-4145-06

Product NDC: 51672-4145

Manufacturer
Sun Pharmaceutical Industries, Inc.
Dosage Form
Cream
Route
Topical
Product Type
Human Prescription Drug
Marketing Start
April 15, 2011
Listing Expires
December 31, 2026
Application
ANDA200173
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Active Ingredients

IngredientStrength
Imiquimod50 mg/g

Drug Class

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

Selected Package

51672-4145-06Selected

24 PACKET in 1 CARTON (51672-4145-6) / .25 g in 1 PACKET (51672-4145-8)