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
24658-703_8e09c72c-3a37-4b5f-882d-70df65ef558e
Product NDC
24658-703
Form
TABLET
Composition / generic term
ESTRADIOL
Labeler
PURACAP LABORATORIES, LLC
Marketing category
ANDA
Marketing start / end (source format)
20210910
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 (24658-703-01) · 24658-703-01
  • 500 TABLET in 1 BOTTLE (24658-703-05) · 24658-703-05

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.

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