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
70518-3818_53c1f4fc-2044-c013-e063-6394a90a744e
Product NDC
70518-3818
Form
TABLET
Composition / generic term
ESTRADIOL
Labeler
REMEDYREPACK INC.
Marketing category
ANDA
Marketing start / end (source format)
20230803
Source listing expiry
20271231

Source-listed ingredients

  • ESTRADIOL — 1 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 90 TABLET in 1 BOTTLE, PLASTIC (70518-3818-0) · 70518-3818-0
  • 100 POUCH in 1 BOX (70518-3818-1) / 1 TABLET in 1 POUCH (70518-3818-2) · 70518-3818-1

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 →