# EUTHYROX

NDC: 72305-075
Generic name: levothyroxine sodium
Labeler / Manufacturer: Provell Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20181017
Marketing ended: 20260930
FDA application: NDA021292

## Active ingredients

- LEVOTHYROXINE SODIUM: 75 ug/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72305-075"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72305-075
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bc3c6830-ba68-4ba3-9896-a12d0ad0b275