Mupirocin
- Product NDC
- 63187-015
- 11-digit product format
- 631870015
- Labeler code
- 63187
- Product ID
- 63187-015_141d8892-7f38-43d4-8bc4-5a0bf6198717
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mupirocin
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Proficient Rx LP
- Application
- ANDA090480
- Marketing category
- ANDA
- Marketing start
- 2011-06-08
- 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 |
|---|
| 63187-015-22 | Mupirocin | 22 g in 1 TUBE | OINTMENT | 22 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63187-015 | MUPIROCIN OINTMENT [PROFICIENT RX LP] | 4 | Current NDC, Legacy NDC, 1 package rows | 20231109_2777e4f2-2b8d-41f5-a96a-02dec8c7c3e0.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 |
|---|
| 63187-015-22 | 63187001522 | 22 g in 1 TUBE (63187-015-22) | 22 g | 2018-11-01 | 0000-00-00 | No | No | Current |