# Levothyroxine Sodium

NDC: 82804-277
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: 20190320

FDA application: ANDA209713

## Active ingredients

- LEVOTHYROXINE SODIUM: .112 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"82804-277"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82804-277
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7d07e932-7372-4c17-aa53-55087107fa52