NDC 51672-1318 – Ciclopirox Olamine
Ciclopirox Olamine 7.7 mg/g · Cream · Topical
Product NDC51672-1318
Product details
- Brand name
- Ciclopirox Olamine
- Generic name
- Ciclopirox olamine
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Cream
- Route
- Topical
- Marketing category
- ANDA · ANDA076790
- Marketed since
- April 12, 2005
- Listing expires
- December 31, 2027
Active ingredients
- Ciclopirox Olamine 7.7 mg/g
Uses, dosage, side effects and warnings for Ciclopirox olamine →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 51672-1318-1 | 1 TUBE in 1 CARTON (51672-1318-1) / 15 g in 1 TUBE | Apr 12, 2005 |
| 51672-1318-2 | 1 TUBE in 1 CARTON (51672-1318-2) / 30 g in 1 TUBE | Apr 12, 2005 |
| 51672-1318-8 | 1 TUBE in 1 CARTON (51672-1318-8) / 90 g in 1 TUBE | Apr 12, 2005 |
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