Estradiol

Product NDC
50090-7480
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Estradiol
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA217334
Marketing category
ANDA
Substance
ESTRADIOL
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-7480-030 TABLET in 1 BOTTLE (50090-7480-0) 2024-12-20NoHistorical
50090-7480-290 TABLET in 1 BOTTLE (50090-7480-2) 2024-12-20NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Estradiol Tablets, USP Rx onlyA-S Medication Solutions2024-12-30HUMAN PRESCRIPTION DRUG LABEL1