Levothyroxine sodium

Product NDC
71335-1945
11-digit product format
713351945
Labeler code
71335
Product ID
71335-1945_0b0aea3a-ded7-4179-bb60-5df8650fa2e2
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Levothyroxine Sodium
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA212399
Marketing category
ANDA
Marketing start
2020-12-03
Substance
LEVOTHYROXINE SODIUM
Active strength
125 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
71335-1945-17133519450130 TABLET in 1 BOTTLE (71335-1945-1) 30 tablet2021-11-23NoNoHistorical
71335-1945-271335194502100 TABLET in 1 BOTTLE (71335-1945-2) 100 tablet2024-12-11NoNoHistorical
71335-1945-37133519450390 TABLET in 1 BOTTLE (71335-1945-3) 90 tablet2021-10-27NoNoHistorical
71335-1945-47133519450460 TABLET in 1 BOTTLE (71335-1945-4) 60 tablet2024-12-11NoNoHistorical
71335-1945-57133519450528 TABLET in 1 BOTTLE (71335-1945-5) 28 tablet2024-12-11NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Levothyroxine sodiumBryant Ranch Prepack2024-12-11HUMAN PRESCRIPTION DRUG LABEL104