Mupirocin
- Product NDC
- 68788-7993
- 11-digit product format
- 687887993
- Labeler code
- 68788
- Product ID
- 68788-7993_71493ba6-bddc-4c66-9f22-d4edd31250b8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mupirocin
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA065170
- Marketing category
- ANDA
- Marketing start
- 2021-08-09
- 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 Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68788-7993 | MUPIROCIN OINTMENT [PREFERRED PHARMACEUTICALS INC.] | 4 | Legacy NDC | 20240724_cd1f69fd-54fe-45e3-b80e-ac1f445415d5.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7993-2 | 68788799302 | 1 TUBE in 1 CARTON (68788-7993-2) > 22 g in 1 TUBE | 1 tube | 2021-08-09 | 0000-00-00 | No | No | Current |