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: 71205-222_aca8c79e-06fa-4919-bc65-a2aff5429fde
Product NDC: 71205-222
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 — .112 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

30 TABLET in 1 BOTTLE, PLASTIC (71205-222-30) · 71205-222-30
60 TABLET in 1 BOTTLE, PLASTIC (71205-222-60) · 71205-222-60
90 TABLET in 1 BOTTLE, PLASTIC (71205-222-90) · 71205-222-90

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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