Mupirocin
- Product NDC
- 70518-2344
- 11-digit product format
- 705182344
- Labeler code
- 70518
- Product ID
- 70518-2344_e39b3c9e-e83e-6b45-e053-2995a90ad9b3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mupirocin
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA065170
- Marketing category
- ANDA
- Marketing start
- 2019-10-04
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2344-0 | 70518234400 | 1 TUBE in 1 CARTON (70518-2344-0) > 22 g in 1 TUBE | 1 tube | 2019-10-04 | 0000-00-00 | No | No | Current |
| 70518-2344-1 | 70518234401 | 1 TUBE in 1 CARTON (70518-2344-1) > 15 g in 1 TUBE | 1 tube | 2020-08-12 | 0000-00-00 | No | No | Current |