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
- 68071-3887_47cfe577-b4ca-d35e-e063-6394a90ad8c4
- Product NDC
- 68071-3887
- Form
- TABLET
- Composition / generic term
- LEVOTHYROXINE SODIUM
- Labeler
- NuCare Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250408
- 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 (68071-3887-3) · 68071-3887-3
- 90 TABLET in 1 BOTTLE (68071-3887-9) · 68071-3887-9
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →