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
71335-1940_3ba1753b-b511-4832-90e0-2284225e535a
Product NDC
71335-1940
Form
TABLET
Composition / generic term
Levothyroxine Sodium
Labeler
Bryant Ranch Prepack
Marketing category
NDA AUTHORIZED GENERIC
Marketing start / end (source format)
20200803
Source listing expiry
20261231

Source-listed ingredients

  • LEVOTHYROXINE SODIUM — 200 ug/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE (71335-1940-1) · 71335-1940-1
  • 30 TABLET in 1 BOTTLE (71335-1940-2) · 71335-1940-2
  • 90 TABLET in 1 BOTTLE (71335-1940-3) · 71335-1940-3
  • 60 TABLET in 1 BOTTLE (71335-1940-4) · 71335-1940-4
  • 18 TABLET in 1 BOTTLE (71335-1940-5) · 71335-1940-5

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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