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
68071-3956_491369a9-b7bc-43d9-e063-6294a90ad1e4
Product NDC
68071-3956
Form
TABLET
Composition / generic term
Levothyroxine Sodium
Labeler
NuCare Pharmaceuticals, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20190320
Source listing expiry
20271231

Source-listed ingredients

  • LEVOTHYROXINE SODIUM — .025 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 90 TABLET in 1 BOTTLE (68071-3956-9) · 68071-3956-9

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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