Mupirocin
- Product NDC
- 53002-9852
- 11-digit product format
- 530029852
- Labeler code
- 53002
- Product ID
- 53002-9852_821c42fe-5fb4-4eb6-a256-281dc3440ea4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mupirocin
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- RPK Pharmaceuticals, Inc.
- Application
- ANDA065085
- Marketing category
- ANDA
- Marketing start
- 2003-11-07
- Marketing end
- 0000-00-00
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
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 |
|---|
| 53002-9852-1 | Mupirocin | 22 g in 1 TUBE | OINTMENT | 22 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53002-9852 | MUPIROCIN OINTMENT [RPK PHARMACEUTICALS, INC.] | 1 | Legacy NDC, 1 package rows | 20201224_9a44afdd-e127-47a1-8ba6-3ab2e20936c5.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 |
|---|
| 53002-9852-1 | 53002985201 | 22 g in 1 TUBE (53002-9852-1) | 22 g | 2019-01-01 | 0000-00-00 | No | No | Current |