Estradiol

Product NDC
71335-2387
11-digit product format
713352387
Labeler code
71335
Product ID
71335-2387_163b7c0d-6b69-4ca2-bc23-b60e268bc176
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
1 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
71335-2387-171335238701100 TABLET in 1 BOTTLE (71335-2387-1) 100 tablet2024-07-08NoNoHistorical
71335-2387-27133523870230 TABLET in 1 BOTTLE (71335-2387-2) 30 tablet2024-07-08NoNoHistorical
71335-2387-37133523870390 TABLET in 1 BOTTLE (71335-2387-3) 90 tablet2024-07-08NoNoHistorical
71335-2387-47133523870460 TABLET in 1 BOTTLE (71335-2387-4) 60 tablet2024-07-08NoNoHistorical
71335-2387-571335238705180 TABLET in 1 BOTTLE (71335-2387-5) 180 tablet2024-07-08NoNoHistorical
71335-2387-671335238706120 TABLET in 1 BOTTLE (71335-2387-6) 120 tablet2024-07-08NoNoHistorical
71335-2387-77133523870728 TABLET in 1 BOTTLE (71335-2387-7) 28 tablet2024-07-08NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Estradiol Tablets, USP Rx onlyBryant Ranch Prepack2024-07-08HUMAN PRESCRIPTION DRUG LABEL1