# Levothyroxine sodium

NDC: 71205-681
Generic name: Levothyroxine Sodium
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20201203

FDA application: ANDA212399

## Active ingredients

- LEVOTHYROXINE SODIUM: 125 ug/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71205-681"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71205-681
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2f129a3d-f3e6-45b2-9704-3ad171cbd8a5