United States · FDA National Drug Code directory

Synthroid

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
0074-6594_b85ab7fa-ba96-43cd-b736-44b3924e644c
Product NDC
0074-6594
Form
TABLET
Composition / generic term
Levothyroxine Sodium
Labeler
AbbVie Inc.
Marketing category
NDA
Marketing start / end (source format)
20020724
Source listing expiry
20261231

Source-listed ingredients

  • LEVOTHYROXINE SODIUM — 88 ug/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1000 TABLET in 1 BOTTLE (0074-6594-19) · 0074-6594-19
  • 2 BLISTER PACK in 1 CARTON (0074-6594-72) / 7 TABLET in 1 BLISTER PACK · 0074-6594-72
  • 90 TABLET in 1 BOTTLE (0074-6594-90) · 0074-6594-90

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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