Mupirocin
- Product NDC
- 50268-568
- 11-digit product format
- 502680568
- Labeler code
- 50268
- Product ID
- 50268-568_48d41df2-2bbc-ccd4-e063-6294a90a2c50
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mupirocin
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- AvPAK
- Application
- ANDA065170
- Marketing category
- ANDA
- Marketing start
- 2019-06-11
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Mupirocin
- Listing expiration
- 2027-12-31
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 |
|---|
| 50268-568-11 | Mupirocin | 50 g in 1 TUBE | OINTMENT | 50 | | 7 |
| 50268-568-15 | Mupirocin | 50 in 1 BOX | OINTMENT | 50 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50268-568 | MUPIROCIN OINTMENT [AVPAK] | 5 | Current NDC, Legacy NDC, 2 package rows | 20250313_8b10c706-ae9c-fc76-e053-2a95a90a4c73.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50268-568-11 | 50268056811 | 50 g in 1 TUBE | 50 g | | | | | Historical |
| 50268-568-15 | 50268056815 | 50 TUBE in 1 BOX (50268-568-15) / 50 g in 1 TUBE (50268-568-11) | 50 tube | 2019-06-11 | 0000-00-00 | No | No | Current |