Levothyroxine Sodium

Product NDC
50090-6594
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Levothyroxine Sodium
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
NDA021342
Marketing category
NDA AUTHORIZED GENERIC
Substance
LEVOTHYROXINE SODIUM
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-6594-090 TABLET in 1 BOTTLE (50090-6594-0) 2023-08-18NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Levothyroxine SodiumA-S Medication Solutions2023-09-14HUMAN PRESCRIPTION DRUG LABEL8