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
- 71335-1827_99522782-da02-4402-b98a-40b831694bf8
- Product NDC
- 71335-1827
- Form
- TABLET
- Composition / generic term
- Levothyroxine Sodium
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20201125
- Source listing expiry
- 20271231
Source-listed ingredients
- LEVOTHYROXINE SODIUM — 75 ug/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (71335-1827-1) · 71335-1827-1
- 100 TABLET in 1 BOTTLE (71335-1827-2) · 71335-1827-2
- 60 TABLET in 1 BOTTLE (71335-1827-3) · 71335-1827-3
- 90 TABLET in 1 BOTTLE (71335-1827-4) · 71335-1827-4
- 28 TABLET in 1 BOTTLE (71335-1827-5) · 71335-1827-5
- 10 TABLET in 1 BOTTLE (71335-1827-6) · 71335-1827-6
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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