NDC 51672-4145 – Imiquimod
Imiquimod 50 mg/g · Cream · Topical
Product NDC51672-4145
Product details
- Brand name
- Imiquimod
- Generic name
- Imiquimod
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Cream
- Route
- Topical
- Marketing category
- ANDA · ANDA200173
- Marketed since
- April 15, 2011
- Listing expires
- December 31, 2026
Active ingredients
- Imiquimod 50 mg/g
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 51672-4145-6 | 24 PACKET in 1 CARTON (51672-4145-6) / .25 g in 1 PACKET (51672-4145-8) | Apr 15, 2011 |
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