FDA.reportPublic FDA data

Mupirocin

Product NDC
42254-137
11-digit product format
422540137
Labeler code
42254
Product ID
42254-137_323bcad0-1e11-4946-a151-1a33557f0bfb
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Mupirocin
Dosage form
OINTMENT
Route
TOPICAL
Labeler
Rebel Distributors Corp
Application
ANDA065085
Marketing category
ANDA
Marketing start
2011-01-11
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
2017-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f2f8c312-f164-6104-0de4-ec45484840e3Product name220260304
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
0c2e0212-b823-4ce8-611e-853ac2cac1b2Product name420230327
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
3db2f5c1-f78c-f062-515c-4827e36c2518Product name120140508
d723478e-ad4a-ec23-6bd7-cfe33e1e3840Product name120140508
f74f326b-f453-01a0-e7e7-ce5ea9475503Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
42254-137-222019-09-24C16284748780-19350213a-3d70-c013-e053-90daa90a1393MUPIROCIN OINTMENT USP, 2% 1010 For Dermatologic Use

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
42254-137-22Mupirocin22 g in 1 TUBEOINTMENT221

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
42254-137-22GM - Gram42254-137d7993286-090f-49b9-991f-608288913a9f12012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
MUPIROCINACTIVE INGREDIENTD0GX863OA5MUPIROCIN OINTMENT [REBEL DISTRIBUTORS CORP]1
MUPIROCINACTIVE MOIETYD0GX863OA5MUPIROCIN OINTMENT [REBEL DISTRIBUTORS CORP]1
POLYETHYLENE GLYCOL 3350INACTIVE INGREDIENTG2M7P15E5PMUPIROCIN OINTMENT [REBEL DISTRIBUTORS CORP]1
POLYETHYLENE GLYCOL 400INACTIVE INGREDIENTB697894SGQMUPIROCIN OINTMENT [REBEL DISTRIBUTORS CORP]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
42254-137MUPIROCIN OINTMENT [REBEL DISTRIBUTORS CORP]1Legacy NDC, 1 package rows20120420_323bcad0-1e11-4946-a151-1a33557f0bfb.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
106346mupirocin 2 % Topical OintmentPSN323bcad0-1e11-4946-a151-1a33557f0bfb1
106346mupirocin 0.02 MG/MG Topical OintmentSCD323bcad0-1e11-4946-a151-1a33557f0bfb1
106346mupirocin 2 % Topical OintmentSY323bcad0-1e11-4946-a151-1a33557f0bfb1
106346mupirocin 20 MG per GM Topical OintmentSY323bcad0-1e11-4946-a151-1a33557f0bfb1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
42254-137-224225401372222 g in 1 TUBE22 gHistorical