mupirocin
- Product NDC
- 53002-9853
- 11-digit product format
- 530029853
- Labeler code
- 53002
- Product ID
- 53002-9853_8d3c133a-e784-446b-b822-e59c590e4db3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mupirocin
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- RPK Pharmaceuticals, Inc.
- Application
- ANDA065123
- Marketing category
- ANDA
- Marketing start
- 2009-10-30
- 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
- 2023-12-31
- 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 |
|---|
| 53002-9853-1 | 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 |
|---|
| 53002-9853 | MUPIROCIN OINTMENT [RPK PHARMACEUTICALS, INC.] | 1 | Legacy NDC, 1 package rows | 20220331_f876784e-5542-4e9c-adc5-a65b038462d9.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 |
|---|
| 53002-9853-1 | 53002985301 | 22 g in 1 TUBE (53002-9853-1) | 22 g | 2021-01-01 | 0000-00-00 | No | No | Current |