Estradiol

Product NDC
68071-3629
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Estradiol
Dosage form
TABLET
Route
ORAL
Labeler
NuCare Pharmaceuticals,Inc.
Application
ANDA217334
Marketing category
ANDA
Substance
ESTRADIOL
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
68071-3629-330 TABLET in 1 BOTTLE (68071-3629-3) 2024-06-25NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Estradiol Tablets, USP Rx onlyNuCare Pharmaceuticals,Inc.2024-06-25HUMAN PRESCRIPTION DRUG LABEL1