MUPIROCIN
- Product NDC
- 71589-015
- 11-digit product format
- 715890015
- Labeler code
- 71589
- Product ID
- 71589-015_4182dbe3-d821-4708-89a0-1f85ff0d4a0f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- MUPIROCIN
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Aleor Dermaceuticals Limited
- Application
- ANDA213053
- Marketing category
- ANDA
- Marketing start
- 2021-12-01
- Marketing end
- 0000-00-00
- Substance
- MUPIROCIN CALCIUM
- Active strength
- 20 mg/g
- Pharmacologic classes
- RNA Synthetase Inhibitor Antibacterial [EPC],RNA Synthetase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71589-015-15 | 71589001515 | 1 TUBE in 1 CARTON (71589-015-15) > 15 g in 1 TUBE | 1 tube | 2021-12-01 | 0000-00-00 | No | No | Current |
| 71589-015-30 | 71589001530 | 1 TUBE in 1 CARTON (71589-015-30) > 30 g in 1 TUBE | 1 tube | 2021-12-01 | 0000-00-00 | No | No | Current |