NDC 51672-4174 – Imiquimod
Imiquimod 37.5 mg/g · Cream · Topical
Product NDC51672-4174
Product details
- Brand name
- Imiquimod
- Generic name
- Imiquimod
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Cream
- Route
- Topical
- Marketing category
- ANDA · ANDA205971
- Marketed since
- January 26, 2021
- Listing expires
- December 31, 2027
Active ingredients
- Imiquimod 37.5 mg/g
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 51672-4174-6 | 28 PACKET in 1 CARTON (51672-4174-6) / .25 g in 1 PACKET (51672-4174-8) | Jan 26, 2021 |
| 51672-4174-9 | 1 BOTTLE, PUMP in 1 CARTON (51672-4174-9) / 7.5 g in 1 BOTTLE, PUMP | Oct 14, 2021 |
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