mupirocin
- Product NDC
- 70518-1808
- 11-digit product format
- 705181808
- Labeler code
- 70518
- Product ID
- 70518-1808_49760a72-901f-99dd-e063-6394a90a5cf9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mupirocin
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA065123
- Marketing category
- ANDA
- Marketing start
- 2019-01-21
- 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#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-1808-0 | mupirocin | 1 in 1 CARTON | OINTMENT | 1 | | 8 |
| 70518-1808-0 | mupirocin | 22 g in 1 TUBE | OINTMENT | 22 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-1808 | MUPIROCIN OINTMENT [REMEDYREPACK INC.] | 6 | Current NDC, Legacy NDC, 2 package rows | 20250228_290b4e51-59b4-429a-987b-715ac817ef2c.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 |
|---|
| 70518-1808-0 | 70518180800 | 1 TUBE in 1 CARTON (70518-1808-0) / 22 g in 1 TUBE | 1 tube | 2019-01-21 | 0000-00-00 | No | No | Current |