MUPIROCIN
- Product NDC
- 61919-158
- 11-digit product format
- 619190158
- Labeler code
- 61919
- Product ID
- 61919-158_4d7625bb-db93-7369-e063-6394a90a679f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- MUPIROCIN
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- DIRECT RX
- Application
- ANDA065085
- Marketing category
- ANDA
- Marketing start
- 2014-01-01
- 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#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 61919-158-22 | MUPIROCIN | 20 g in 1 TUBE | OINTMENT | 20 | | 4 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-158 | MUPIROCIN OINTMENT [DIRECT RX] | 3 | Current NDC, Legacy NDC, 1 package rows | 20200122_f88eea1a-2ba1-48bf-96c8-d96d18752aaa.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 |
|---|
| 61919-158-22 | 61919015822 | 20 g in 1 TUBE (61919-158-22) | 20 g | 2015-01-01 | 0000-00-00 | No | No | Current |