# Levothyroxine Sodium

NDC: 67046-0517
Generic name: Levothyroxine Sodium
Labeler / Manufacturer: Coupler LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20260601

FDA application: ANDA209713

## Active ingredients

- LEVOTHYROXINE SODIUM: .175 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"67046-0517"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67046-0517
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=53316e75-9897-4935-e063-6294a90a94cf