Levothyroxine sodium

Product NDC
50090-6090
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Levothyroxine Sodium
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA212399
Marketing category
ANDA
Substance
LEVOTHYROXINE SODIUM
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-6090-030 TABLET in 1 BOTTLE (50090-6090-0) 2022-09-21NoHistorical
50090-6090-190 TABLET in 1 BOTTLE (50090-6090-1) 2022-09-21NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Levothyroxine sodiumA-S Medication Solutions2023-11-16HUMAN PRESCRIPTION DRUG LABEL3