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: 71205-240_71aa09de-da41-40e4-8d5c-28cf1da86064
Product NDC: 71205-240
Form: TABLET
Composition / generic term: Levothyroxine Sodium
Labeler: Proficient Rx LP
Marketing category: NDA
Marketing start / end (source format): 20031201
Source listing expiry: 20261231

Source-listed ingredients

LEVOTHYROXINE SODIUM — .1 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

30 TABLET in 1 BOTTLE, PLASTIC (71205-240-30) · 71205-240-30
60 TABLET in 1 BOTTLE, PLASTIC (71205-240-60) · 71205-240-60
90 TABLET in 1 BOTTLE, PLASTIC (71205-240-90) · 71205-240-90

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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