# Levothyroxine Sodium

NDC: 71205-221
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: 20031201

FDA application: NDA021210

## Active ingredients

- LEVOTHYROXINE SODIUM: .025 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71205-221"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71205-221
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2f0657d5-3e5c-4249-bfaa-7f5ef1528672