FDA.reportPublic FDA data

LEVOTHYROXINE

Product NDC
51655-290
11-digit product format
516550290
Labeler code
51655
Product ID
51655-290_64f1daf6-af49-4087-a874-974fed3ecb79
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
LEVOTHYROXINE
Dosage form
TABLET
Route
ORAL
Labeler
Northwind Pharmaceuticals, LLC
Application
NDA021210
Marketing category
NDA AUTHORIZED GENERIC
Marketing start
2014-09-14
Marketing end
0000-00-00
Substance
LEVOTHYROXINE SODIUM
Active strength
125 ug/1
Pharmacologic classes
l-Thyroxine [EPC],Thyroxine [CS]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51655-290-522026-01-07C16284748780-19d75b9d0-f87a-f424-e053-dadaa90a57cebd1ce5e4-9dd5-4bd5-ae5e-c88822c04f98
51655-290-522020-01-31C16284748780-19d75b9d0-f87a-f424-e053-dadaa90a57cebd1ce5e4-9dd5-4bd5-ae5e-c88822c04f98

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
LEVOTHYROXINE SODIUMACTIVE INGREDIENT9J765S329GLEVOTHYROXINE TABLET [NORTHWIND PHARMACEUTICALS, LLC]1
LEVOTHYROXINEACTIVE MOIETYQ51BO43MG4LEVOTHYROXINE TABLET [NORTHWIND PHARMACEUTICALS, LLC]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51655-290LEVOTHYROXINE TABLET [NORTHWIND PHARMACEUTICALS, LLC]1Legacy NDC20140924_bd1ce5e4-9dd5-4bd5-ae5e-c88822c04f98.zip