Mupirocin
- Product NDC
- 0168-0352
- 11-digit product format
- 001680352
- Labeler code
- 0168
- Product ID
- 0168-0352_edf46c09-0326-4bb1-90bb-0bd3715600c5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- mupirocin
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.
- Application
- ANDA065192
- Marketing category
- ANDA
- Marketing start
- 2005-11-30
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Socrata Ingredients#
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 |
|---|
| 0168-0352-22 | 00168035222 | 22 g in 1 TUBE (0168-0352-22) | 22 g | 2005-11-30 | 0000-00-00 | No | No | Current |