United States · FDA National Drug Code directory
EUTHYROX
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
- 72305-150_8b98dc0b-b9fa-42eb-81a0-07b4679d9332
- Product NDC
- 72305-150
- Form
- TABLET
- Composition / generic term
- levothyroxine sodium
- Labeler
- Provell Pharmaceuticals, LLC
- Marketing category
- NDA
- Marketing start / end (source format)
- 20181017 / 20260930
Source-listed ingredients
- LEVOTHYROXINE SODIUM — 150 ug/1
These values do not establish equivalence or a dose recommendation.
Packages
- 2 BLISTER PACK in 1 CARTON (72305-150-30) / 15 TABLET in 1 BLISTER PACK · 72305-150-30
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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