# Levothyroxine sodium

NDC: 68788-7953
Generic name: Levothyroxine Sodium
Labeler / Manufacturer: Preferred Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20210709

FDA application: ANDA212399

## Active ingredients

- LEVOTHYROXINE SODIUM: 150 ug/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68788-7953"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-7953
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4f40db1e-3dd9-4c7b-93e6-64f0fd10d551