Methimazole

Product NDC
50090-6536
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Methimazole
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA040734
Marketing category
ANDA
Substance
METHIMAZOLE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-6536-090 TABLET in 1 BOTTLE (50090-6536-0) 2023-06-28NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Rx onlyA-S Medication Solutions2023-06-29HUMAN PRESCRIPTION DRUG LABEL1