United States · FDA National Drug Code directory

LEVOTHYROXINE SODIUM

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
72189-155_1922dbd9-96de-8652-e063-6294a90a0afe
Product NDC
72189-155
Form
TABLET
Composition / generic term
LEVOTHYROXINE SODIUM
Labeler
DIRECT RX
Marketing category
NDA
Marketing start / end (source format)
20201201
Source listing expiry
20261231

Source-listed ingredients

  • LEVOTHYROXINE SODIUM — 50 ug/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET in 1 BOTTLE (72189-155-30) · 72189-155-30
  • 90 TABLET in 1 BOTTLE (72189-155-90) · 72189-155-90

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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