United States · FDA National Drug Code directory

Liothyronine 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
87063-080_4a5e9691-7284-6bcd-e063-6294a90aadfc
Product NDC
87063-080
Form
TABLET
Composition / generic term
Liothyronine Sodium
Labeler
ASCLEMED USA INC.
Marketing category
ANDA
Marketing start / end (source format)
20121203
Source listing expiry
20271231

Source-listed ingredients

  • LIOTHYRONINE SODIUM — 5 ug/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1000 TABLET in 1 BOTTLE (87063-080-00) · 87063-080-00
  • 100 TABLET in 1 BOTTLE (87063-080-01) · 87063-080-01
  • 30 TABLET in 1 BOTTLE (87063-080-30) · 87063-080-30
  • 60 TABLET in 1 BOTTLE (87063-080-60) · 87063-080-60
  • 90 TABLET in 1 BOTTLE (87063-080-90) · 87063-080-90

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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