mupirocin
- Product NDC
- 52959-743
- 11-digit product format
- 529590743
- Labeler code
- 52959
- Product ID
- 52959-743_09fcfeb2-8e52-4417-86b5-63688d9ede45
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mupirocin
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- H.J. Harkins Company, Inc.
- Application
- ANDA065123
- Marketing category
- ANDA
- Marketing start
- 2009-10-30
- 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
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 52959-743-22 | mupirocin | 1 in 1 CARTON | OINTMENT | 1 | | 1 |
| 52959-743-22 | mupirocin | 22 g in 1 TUBE | OINTMENT | 22 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52959-743 | MUPIROCIN OINTMENT [H.J. HARKINS COMPANY, INC.] | 1 | Legacy NDC, 2 package rows | 20111205_6a0b39c0-c207-4efc-ac2c-07506ad796df.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 52959-743-22 | 52959074322 | 1 in 1 CARTON | Historical |