# Levothyroxine Sodium

NDC: 83270-007
Generic name: LEVOTHYROXINE SODIUM ANHYDROUS
Labeler / Manufacturer: ONESOURCE SPECIALTY PHARMA LIMITED
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20250815

FDA application: ANDA216729

## Active ingredients

- LEVOTHYROXINE SODIUM ANHYDROUS: 200 ug/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"83270-007"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=83270-007
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ae9954a5-e196-449c-abea-ebe4afbee517