NDC 51672-1312 – Mupirocin
Mupirocin 20 mg/g · Ointment · Topical
Product NDC51672-1312
Product details
- Brand name
- Mupirocin
- Generic name
- Mupirocin
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Ointment
- Route
- Topical
- Marketing category
- ANDA · ANDA065170
- Marketed since
- September 23, 2005
- Listing expires
- December 31, 2026
- Pharmacologic class
- RNA Synthetase Inhibitor Antibacterial
Active ingredients
- Mupirocin 20 mg/g
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 51672-1312-0 | 1 TUBE in 1 CARTON (51672-1312-0) / 22 g in 1 TUBE | Sep 23, 2005 |
| 51672-1312-1 | 1 TUBE in 1 CARTON (51672-1312-1) / 15 g in 1 TUBE | Sep 23, 2005 |
| 51672-1312-2 | 1 TUBE in 1 CARTON (51672-1312-2) / 30 g in 1 TUBE | Sep 23, 2005 |
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