mupirocin
- Product NDC
- 71335-2829
- 11-digit product format
- 713352829
- Labeler code
- 71335
- Product ID
- 71335-2829_41ea0113-860c-0690-e063-6294a90a8b86
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mupirocin
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA065123
- Marketing category
- ANDA
- Marketing start
- 2009-10-30
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- mupirocin
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MUPIROCIN | 20 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | D0GX863OA5 |
| Rxcui | 106346 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-2829-1 | mupirocin | 22 g in 1 TUBE | OINTMENT | 22 | | 100 |
| 71335-2829-1 | mupirocin | 1 in 1 CARTON | OINTMENT | 1 | | 100 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2829-1 | 71335282901 | 1 TUBE in 1 CARTON (71335-2829-1) / 22 g in 1 TUBE | 1 tube | 2025-10-23 | No | No | Current |