# LEVOTHYROXINE SODIUM

NDC: 72603-660
Generic name: LEVOTHYROXINE SODIUM
Labeler / Manufacturer: NorthStar RxLLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250408

FDA application: ANDA211417

## 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:"72603-660"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72603-660
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=58f4dc90-3648-49dc-a7e1-baf918a773b5