levothyroxine sodium

Product NDC
71335-1438
11-digit product format
713351438
Labeler code
71335
Product ID
71335-1438_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
88 ug/1
Pharmacologic classes
Thyroxine [CS], l-Thyroxine [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
levothyroxine sodium
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
LEVOTHYROXINE SODIUM88 ug/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii9J765S329G
Rxcui892246, 892251, 966220, 966221, 966222, 966224, 966225, 966248, 966249, 966253, 966270

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-1438-17133514380130 TABLET in 1 BOTTLE (71335-1438-1) 30 tablet2019-12-160000-00-00NoNoCurrent
71335-1438-27133514380290 TABLET in 1 BOTTLE (71335-1438-2) 90 tablet2019-12-160000-00-00NoNoCurrent
71335-1438-37133514380328 TABLET in 1 BOTTLE (71335-1438-3) 28 tablet2019-12-160000-00-00NoNoCurrent
71335-1438-471335143804100 TABLET in 1 BOTTLE (71335-1438-4) 100 tablet2019-12-160000-00-00NoNoCurrent
71335-1438-57133514380560 TABLET in 1 BOTTLE (71335-1438-5) 60 tablet2019-12-160000-00-00NoNoCurrent