Mupirocin
- Product NDC
- 50436-1010
- 11-digit product format
- 504361010
- Labeler code
- 50436
- Product ID
- 50436-1010_e965a8f3-5d07-4e39-a960-ca936504a80a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mupirocin
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Unit Dose Services
- Application
- ANDA065085
- Marketing category
- ANDA
- Marketing start
- 2003-11-07
- 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 |
| 362d7abb-94e6-4c60-9a58-266894157713 | Product name | 1 | 20231023 |
| 0c2e0212-b823-4ce8-611e-853ac2cac1b2 | Product name | 4 | 20230327 |
| 816b97af-edc5-4060-aff1-b814bdbcad50 | Product name | 1 | 20190415 |
| 419aab54-5d5a-4146-9453-026d4a9991be | Product name | 2 | 20170525 |
| 89dac932-b90a-4410-9ab1-84c53e57de25 | Product name | 1 | 20150316 |
| 3db2f5c1-f78c-f062-515c-4827e36c2518 | Product name | 1 | 20140508 |
| d723478e-ad4a-ec23-6bd7-cfe33e1e3840 | 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 |
|---|---|---|---|---|---|
| 50436-1010-1 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-22a6-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 |
|---|---|---|---|---|---|---|
| 50436-1010-1 | Mupirocin | 22 g in 1 TUBE | OINTMENT | 22 | 6 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 50436-1010-1 | GM - Gram | 50436-1010 | 437331dd-e304-45df-be49-bdcbad2dbea0 | 1 | 2016-11-08 |
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 GLYCOL 3350 | INACTIVE INGREDIENT | G2M7P15E5P | MUPIROCIN OINTMENT [UNIT DOSE SERVICES] | 2 | |
| POLYETHYLENE GLYCOL 400 | INACTIVE INGREDIENT | B697894SGQ | MUPIROCIN OINTMENT [UNIT DOSE SERVICES] | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 50436-1010 | MUPIROCIN OINTMENT [UNIT DOSE SERVICES] | 6 | Legacy NDC, 1 package rows | 20170702_71c82fb9-a374-49f8-97e5-a3ace5c42b05.zip |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 106346 | mupirocin 2 % Topical Ointment | PSN | 71c82fb9-a374-49f8-97e5-a3ace5c42b05 | 6 |
| 106346 | mupirocin 0.02 MG/MG Topical Ointment | SCD | 71c82fb9-a374-49f8-97e5-a3ace5c42b05 | 6 |
| 106346 | mupirocin 2 % Topical Ointment | SY | 71c82fb9-a374-49f8-97e5-a3ace5c42b05 | 6 |
| 106346 | mupirocin 20 MG per GM Topical Ointment | SY | 71c82fb9-a374-49f8-97e5-a3ace5c42b05 | 6 |
Packages#
| Package NDC | 11-digit format | Description | Units | Status |
|---|---|---|---|---|
| 50436-1010-1 | 50436101001 | 22 g in 1 TUBE | 22 g | Historical |