# Levothyroxine Sodium

NDC: 82804-246
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: .125 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"82804-246"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82804-246
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bcf10012-8920-4737-92f5-7401ee0c5894