# Liothyronine sodium

NDC: 70771-1608
Generic name: Liothyronine sodium
Labeler / Manufacturer: Zydus Lifesciences Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20210201

FDA application: ANDA214803

## Active ingredients

- LIOTHYRONINE SODIUM: 50 ug/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70771-1608"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70771-1608
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4fb09346-3d30-4a7c-a97c-480d5924997a