Mupirocin
- Product NDC
- 63187-525
- 11-digit product format
- 631870525
- Labeler code
- 63187
- Product ID
- 63187-525_75ec5f25-865b-455a-b8d6-c942abce985a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mupirocin
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Proficient Rx LP
- Application
- ANDA065085
- Marketing category
- ANDA
- Marketing start
- 2003-11-07
- 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 |
|---|
| 63187-525-22 | Mupirocin | 22 g in 1 TUBE | OINTMENT | 22 | | 4 |
| 63187-525-22 | Mupirocin | 1 in 1 CARTON | OINTMENT | 1 | | 4 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63187-525 | MUPIROCIN OINTMENT [PROFICIENT RX LP] | 4 | Current NDC, Legacy NDC, 2 package rows | 20230306_cbb18010-f3b5-4ed7-8c03-c9203f0e360e.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 |
|---|
| 63187-525-22 | 63187052522 | 1 TUBE in 1 CARTON (63187-525-22) / 22 g in 1 TUBE | 1 tube | 2003-11-07 | 0000-00-00 | No | No | Current |