mupirocin
- Product NDC
- 68788-8642
- 11-digit product format
- 687888642
- Labeler code
- 68788
- Product ID
- 68788-8642_a236cb1e-87c0-4456-907e-dfc266642eb3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mupirocin
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA065123
- Marketing category
- ANDA
- Marketing start
- 2024-04-30
- 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
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- mupirocin
- Listing expiration
- 2026-12-31
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 |
|---|
| 68788-8642-2 | mupirocin | 1 in 1 CARTON | OINTMENT | 1 | | 2 |
| 68788-8642-2 | 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 |
|---|
| 68788-8642 | MUPIROCIN OINTMENT [PREFERRED PHARMACEUTICALS INC.] | 1 | Current NDC, 2 package rows | 20240502_6c9cd7fc-b72e-406e-b9aa-0f1bc035b832.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 68788-8642-2 | 68788864202 | 1 TUBE in 1 CARTON (68788-8642-2) / 22 g in 1 TUBE | 1 tube | 2024-04-30 | No | No | Current |