Estradiol

Product NDC
71335-2477
11-digit product format
713352477
Labeler code
71335
Product ID
71335-2477_d916cc09-ac4d-43ea-b50a-6b9a2ca7bcda
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Estradiol
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA217334
Marketing category
ANDA
Marketing start
2023-09-06
Substance
ESTRADIOL
Active strength
2 mg/1
Pharmacologic classes
Estradiol Congeners [CS], Estrogen Receptor Agonists [MoA], Estrogen [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
4TI98Z838EESTRADIOL50-28-2ESTRADIOL

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71335-2477-17133524770130 TABLET in 1 BOTTLE (71335-2477-1) 30 tablet2024-09-03NoNoHistorical
71335-2477-27133524770215 TABLET in 1 BOTTLE (71335-2477-2) 15 tablet2024-09-03NoNoHistorical
71335-2477-37133524770390 TABLET in 1 BOTTLE (71335-2477-3) 90 tablet2024-09-03NoNoHistorical
71335-2477-47133524770460 TABLET in 1 BOTTLE (71335-2477-4) 60 tablet2024-09-03NoNoHistorical
71335-2477-571335247705100 TABLET in 1 BOTTLE (71335-2477-5) 100 tablet2024-09-03NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Estradiol Tablets, USP Rx onlyBryant Ranch Prepack2024-09-03HUMAN PRESCRIPTION DRUG LABEL1