Mupirocin
- Product NDC
- 69150-225
- 11-digit product format
- 691500225
- Labeler code
- 69150
- Product ID
- 69150-225_6e92fe6b-c000-4755-b0e6-ef5beac548de
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mupirocin
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- BIOMES PHARMACEUTICALS LLC
- Application
- ANDA201587
- Marketing category
- ANDA
- Marketing start
- 2016-03-22
- Marketing end
- 0000-00-00
- Substance
- MUPIROCIN CALCIUM
- Active strength
- 2 g/100g
- Pharmacologic classes
- RNA Synthetase Inhibitor Antibacterial [EPC],RNA Synthetase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69150-225-01 | 69150022501 | 15 g in 1 TUBE (69150-225-01) | 15 g | 2016-03-22 | 0000-00-00 | No | No | Current |
| 69150-225-03 | 69150022503 | 30 g in 1 TUBE (69150-225-03) | 30 g | 2019-12-27 | 0000-00-00 | No | No | Current |