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
68788-8648_bd78156a-c5ec-4686-8b61-d97bf0bafae0
Product NDC
68788-8648
Form
TABLET
Composition / generic term
levothyroxine sodium
Labeler
Preferred Pharmaceuticals Inc.
Marketing category
NDA
Marketing start / end (source format)
20240503
Source listing expiry
20261231

Source-listed ingredients

  • LEVOTHYROXINE SODIUM — 25 ug/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET in 1 BOTTLE (68788-8648-3) · 68788-8648-3
  • 90 TABLET in 1 BOTTLE (68788-8648-9) · 68788-8648-9

Source and coverage

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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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