Liothyronine sodium

Product NDC
71335-1943
11-digit product format
713351943
Labeler code
71335
Product ID
71335-1943_ea5f289f-acad-4c98-8e81-82f2d3ed5855
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Liothyronine sodium
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA214803
Marketing category
ANDA
Marketing start
2021-02-01
Substance
LIOTHYRONINE SODIUM
Active strength
25 ug/1
Pharmacologic classes
Triiodothyronine [CS], l-Triiodothyronine [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
LIOTHYRONINE SODIUM25 ug/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiGCA9VV7D2N
Rxcui903697

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-1943-17133519430130 TABLET in 1 BOTTLE (71335-1943-1) 30 tablet2021-11-100000-00-00NoNoCurrent
71335-1943-27133519430228 TABLET in 1 BOTTLE (71335-1943-2) 28 tablet2024-09-060000-00-00NoNoCurrent
71335-1943-37133519430360 TABLET in 1 BOTTLE (71335-1943-3) 60 tablet2021-11-100000-00-00NoNoCurrent
71335-1943-471335194304100 TABLET in 1 BOTTLE (71335-1943-4) 100 tablet2024-09-060000-00-00NoNoCurrent
71335-1943-57133519430590 TABLET in 1 BOTTLE (71335-1943-5) 90 tablet2024-09-060000-00-00NoNoCurrent