levothyroxine sodium

Product NDC
71335-1528
11-digit product format
713351528
Labeler code
71335
Product ID
71335-1528_5dd258ee-53fd-4e60-b3c9-b3cfacd622bf
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
levothyroxine sodium
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
NDA021116
Marketing category
NDA
Marketing start
2019-05-07
Substance
LEVOTHYROXINE SODIUM
Active strength
137 ug/1
Pharmacologic classes
Thyroxine [CS], l-Thyroxine [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
9J765S329GLEVOTHYROXINE SODIUM6106-07-6LEVOTHYROXINE SODIUM

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71335-1528-17133515280130 TABLET in 1 BOTTLE (71335-1528-1) 30 tablet2020-03-05NoNoHistorical
71335-1528-271335152802100 TABLET in 1 BOTTLE (71335-1528-2) 100 tablet2020-03-05NoNoHistorical
71335-1528-37133515280390 TABLET in 1 BOTTLE (71335-1528-3) 90 tablet2020-03-05NoNoHistorical
71335-1528-47133515280428 TABLET in 1 BOTTLE (71335-1528-4) 28 tablet2020-03-05NoNoHistorical
71335-1528-57133515280560 TABLET in 1 BOTTLE (71335-1528-5) 60 tablet2020-03-05NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
levothyroxine sodiumBryant Ranch Prepack2025-07-29HUMAN PRESCRIPTION DRUG LABEL26