# levothyroxine sodium

NDC: 68788-8648
Generic name: levothyroxine sodium
Labeler / Manufacturer: Preferred Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20240503

FDA application: NDA021116

## Active ingredients

- LEVOTHYROXINE SODIUM: 25 ug/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68788-8648"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-8648
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=412fc3f4-d9e0-49c5-b042-a6010aea7e5e