# Levothyroxine sodium

NDC: 71335-1827
Generic name: Levothyroxine Sodium
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20201125

FDA application: ANDA212399

## 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:"71335-1827"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71335-1827
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=775ef7ba-0b5b-40ba-ac7b-2aef121fe4f4