mupirocin
- Product NDC
- 50090-4349
- 11-digit product format
- 500904349
- Labeler code
- 50090
- Product ID
- 50090-4349_f030f896-1c9c-4752-be60-927f87f8a1f7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mupirocin
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- A-S Medication Solutions
- 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
- 2022-12-31
- 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 |
|---|
| 50090-4349-0 | mupirocin | 22 g in 1 TUBE | OINTMENT | 22 | | 1 |
| 50090-4349-0 | mupirocin | 1 in 1 CARTON | OINTMENT | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-4349 | MUPIROCIN OINTMENT [A-S MEDICATION SOLUTIONS] | 1 | Legacy NDC, 2 package rows | 20210602_0b57affe-8fa3-4517-adfd-1b0d938e72eb.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 |
|---|
| 50090-4349-0 | 50090434900 | 1 TUBE in 1 CARTON (50090-4349-0) > 22 g in 1 TUBE | 1 tube | 2019-06-12 | 0000-00-00 | No | No | Current |