mupirocin
- Product NDC
- 68788-8642
- 11-digit product format
- 687888642
- Labeler code
- 68788
- Product ID
- 68788-8642_a236cb1e-87c0-4456-907e-dfc266642eb3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mupirocin
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA065123
- Marketing category
- ANDA
- Marketing start
- 2024-04-30
- Substance
- MUPIROCIN
- Active strength
- 20 mg/g
- Pharmacologic classes
- RNA Synthetase Inhibitor Antibacterial [EPC], RNA Synthetase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| D0GX863OA5 | MUPIROCIN | 12650-69-0 | MUPIROCIN |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 68788-8642-2 | 68788864202 | 1 TUBE in 1 CARTON (68788-8642-2) / 22 g in 1 TUBE | 1 tube | 2024-04-30 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| mupirocin | Preferred Pharmaceuticals Inc. | 2025-08-18 | HUMAN PRESCRIPTION DRUG LABEL | 2 |