Mupirocin
- Product NDC
- 76413-158
- 11-digit product format
- 764130158
- Labeler code
- 76413
- Product ID
- 76413-158_2dfae7d1-39e3-4b94-8d1b-67f5849db239
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mupirocin
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Central Texas Community Health Centers
- Application
- ANDA090480
- Marketing category
- ANDA
- Marketing start
- 2011-06-08
- 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
- 2019-12-31
- 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 |
|---|
| 76413-158-22 | Mupirocin | 22 g in 1 TUBE | OINTMENT | 22 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76413-158 | MUPIROCIN OINTMENT [CENTRAL TEXAS COMMUNITY HEALTH CENTERS] | 2 | Legacy NDC, 1 package rows | 20180426_17c7a199-2e21-4060-9543-3f538108e6b0.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 76413-158-22 | 76413015822 | 22 g in 1 TUBE | 22 g | Historical |