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
- 83270-008_58da3dc9-3dea-30eb-e063-6294a90ad6ea
- Product NDC
- 83270-008
- Form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Composition / generic term
- LEVOTHYROXINE SODIUM ANHYDROUS
- Labeler
- ONESOURCE SPECIALTY PHARMA LIMITED
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260427
- Source listing expiry
- 20271231
Source-listed ingredients
- LEVOTHYROXINE SODIUM ANHYDROUS — 500 ug/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL, SINGLE-DOSE in 1 CARTON (83270-008-01) / 5 mL in 1 VIAL, SINGLE-DOSE · 83270-008-01
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 →