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
- 71205-642_7a6abcab-a753-4c1d-92fb-c134ffc2c0a7
- Product NDC
- 71205-642
- Form
- TABLET
- Composition / generic term
- Levothyroxine Sodium
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20201210
- Source listing expiry
- 20261231
Source-listed ingredients
- LEVOTHYROXINE SODIUM — 100 ug/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (71205-642-30) · 71205-642-30
- 60 TABLET in 1 BOTTLE (71205-642-60) · 71205-642-60
- 90 TABLET in 1 BOTTLE (71205-642-90) · 71205-642-90
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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