United States · FDA National Drug Code directory

ESTRADIOL

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
68788-7102_1dc61390-4e83-49e9-b838-571e38fd13b7
Product NDC
68788-7102
Form
TABLET
Composition / generic term
ESTRADIOL
Labeler
Preferred Pharmaceuticals Inc.
Marketing category
ANDA
Marketing start / end (source format)
20180312
Source listing expiry
20261231

Source-listed ingredients

  • ESTRADIOL — 1 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE (68788-7102-1) · 68788-7102-1
  • 30 TABLET in 1 BOTTLE (68788-7102-3) · 68788-7102-3
  • 60 TABLET in 1 BOTTLE (68788-7102-6) · 68788-7102-6
  • 90 TABLET in 1 BOTTLE (68788-7102-9) · 68788-7102-9

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →