mupirocin
- Product NDC
- 50436-0112
- 11-digit product format
- 504360112
- Labeler code
- 50436
- Product ID
- 50436-0112_5f66512a-ef5b-45e8-99df-759b5436586b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mupirocin
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Unit Dose Services
- 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
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| f2f8c312-f164-6104-0de4-ec45484840e3 | Product name | 2 | 20260304 |
| 0c2e0212-b823-4ce8-611e-853ac2cac1b2 | Product name | 4 | 20230327 |
| 3db2f5c1-f78c-f062-515c-4827e36c2518 | Product name | 1 | 20140508 |
| f74f326b-f453-01a0-e7e7-ce5ea9475503 | Product name | 1 | 20140508 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 50436-0112-1 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-41af-a910-e053-dadaa90a0b85 | These highlights do not include all the information needed to use MUPIROCIN OINTMENT safely and effectively. See full prescribing information for MUPIROCIN OINTMENT . MUPIROCIN ointment, for topical use Initial U.S. Approval: 1987 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50436-0112-1 | mupirocin | 1 g in 1 BOTTLE | OINTMENT | 1 | 6 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 50436-0112-1 | GM - Gram | 50436-0112 | bd38b67a-5ab6-4c25-a181-ecb9eb0b56b2 | 1 | 2016-09-02 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| MUPIROCIN | ACTIVE INGREDIENT | D0GX863OA5 | MUPIROCIN OINTMENT [UNIT DOSE SERVICES] | 2 | |
| MUPIROCIN | ACTIVE MOIETY | D0GX863OA5 | MUPIROCIN OINTMENT [UNIT DOSE SERVICES] | 2 | |
| POLYETHYLENE GLYCOLS | INACTIVE INGREDIENT | 3WJQ0SDW1A | MUPIROCIN OINTMENT [UNIT DOSE SERVICES] | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 50436-0112 | MUPIROCIN OINTMENT [UNIT DOSE SERVICES] | 6 | Legacy NDC, 1 package rows | 20180523_ed60d758-dbce-4963-a378-6c8201c3e66f.zip |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 106346 | mupirocin 2 % Topical Ointment | PSN | ed60d758-dbce-4963-a378-6c8201c3e66f | 6 |
| 106346 | mupirocin 0.02 MG/MG Topical Ointment | SCD | ed60d758-dbce-4963-a378-6c8201c3e66f | 6 |
| 106346 | mupirocin 2 % Topical Ointment | SY | ed60d758-dbce-4963-a378-6c8201c3e66f | 6 |
| 106346 | mupirocin 20 MG per GM Topical Ointment | SY | ed60d758-dbce-4963-a378-6c8201c3e66f | 6 |
Packages#
| Package NDC | 11-digit format | Description | Units | Status |
|---|---|---|---|---|
| 50436-0112-1 | 50436011201 | 1 g in 1 BOTTLE | 1 g | Historical |