# levothyroxine sodium

NDC: 71205-351
Generic name: levothyroxine sodium
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20190507

FDA application: NDA021116

## Active ingredients

- LEVOTHYROXINE SODIUM: 100 ug/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71205-351"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71205-351
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=12ccf2fd-ccf0-4bcf-8eee-e2a16c8b44d6