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
- 69238-1836_3a92e520-3da8-43be-9be2-63511c44b735
- Product NDC
- 69238-1836
- Form
- TABLET
- Composition / generic term
- Levothyroxine Sodium
- Labeler
- Amneal Pharmaceuticals NY LLC
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 20031201
- Source listing expiry
- 20261231
Source-listed ingredients
- LEVOTHYROXINE SODIUM — .125 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE, PLASTIC (69238-1836-1) · 69238-1836-1
- 1000 TABLET in 1 BOTTLE, PLASTIC (69238-1836-7) · 69238-1836-7
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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