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
- 68788-7698_0a8d16fa-f48c-44c3-b0b4-5e16b7e59421
- Product NDC
- 68788-7698
- Form
- TABLET
- Composition / generic term
- levothyroxine sodium
- Labeler
- Preferred Pharmaceuticals, Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20200401
- Source listing expiry
- 20271231
Source-listed ingredients
- LEVOTHYROXINE SODIUM — 50 ug/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (68788-7698-3) · 68788-7698-3
- 90 TABLET in 1 BOTTLE (68788-7698-9) · 68788-7698-9
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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