Liothyronine Sodium

Product NDC
71335-9632
11-digit product format
713359632
Labeler code
71335
Product ID
71335-9632_7e8ca2e4-1c1e-4565-87a1-cd99437d1dac
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Liothyronine Sodium
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA200295
Marketing category
ANDA
Marketing start
2012-12-03
Substance
LIOTHYRONINE SODIUM
Active strength
50 ug/1
Pharmacologic classes
Triiodothyronine [CS], l-Triiodothyronine [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

openFDA Listing Details

Product ID
71335-9632_7e8ca2e4-1c1e-4565-87a1-cd99437d1dac
SPL ID
7e8ca2e4-1c1e-4565-87a1-cd99437d1dac
Product type
HUMAN PRESCRIPTION DRUG
Finished product
Yes
Brand name base
Liothyronine Sodium
Generic name
Liothyronine Sodium
Dosage form
TABLET
Route
ORAL
Marketing start
2012-12-03
Marketing category
ANDA
Application number
ANDA200295
Pharmacologic classes
Triiodothyronine [CS]; l-Triiodothyronine [EPC]
Listing expiration
2026-12-31

openFDA Active Ingredients

IngredientStrength
LIOTHYRONINE SODIUM50 ug/1

openFDA Harmonized Identifiers

FieldValues
UniiGCA9VV7D2N
Rxcui903703
Spl Set Id20cbf84d-80f2-4b94-ad47-6aaa362fb4d0
Manufacturer NameBryant Ranch Prepack

openFDA Package Details

Package NDCDescriptionMarketing startSample
71335-9632-130 TABLET in 1 BOTTLE (71335-9632-1)2023-01-31No

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
GCA9VV7D2NLIOTHYRONINE SODIUM55-06-1LIOTHYRONINE SODIUM

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71335-9632-17133596320130 TABLET in 1 BOTTLE (71335-9632-1) 30 tablet2023-01-31NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Liothyronine SodiumBryant Ranch Prepack2023-11-08HUMAN PRESCRIPTION DRUG LABEL101