Imiquimod 51672-4145
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
| Ingredient | Strength |
|---|---|
| Imiquimod | 50 mg/g |
Drug Class
Increased Cytokine Activity [PE]Increased Cytokine Production [PE]Interferon Inducers [MoA]
Packaging Options(1)
24 PACKET in 1 CARTON (51672-4145-6) / .25 g in 1 PACKET (51672-4145-8)