levothyroxine sodium

Product NDC
71335-1637
11-digit product format
713351637
Labeler code
71335
Product ID
71335-1637_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
175 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
71335-1637-17133516370130 TABLET in 1 BOTTLE (71335-1637-1) 30 tablet2020-06-09NoNoHistorical
71335-1637-27133516370290 TABLET in 1 BOTTLE (71335-1637-2) 90 tablet2020-06-09NoNoHistorical
71335-1637-371335163703100 TABLET in 1 BOTTLE (71335-1637-3) 100 tablet2020-06-09NoNoHistorical
71335-1637-47133516370438 TABLET in 1 BOTTLE (71335-1637-4) 38 tablet2020-06-09NoNoHistorical
71335-1637-57133516370528 TABLET in 1 BOTTLE (71335-1637-5) 28 tablet2020-06-09NoNoHistorical
71335-1637-67133516370660 TABLET in 1 BOTTLE (71335-1637-6) 60 tablet2020-06-09NoNoHistorical

Related DailyMed Labels

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