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Liothyronine sodium

NDC 70771-1607 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Lifesciences Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA214803
Dosage form / routeTABLET · ORAL
Active ingredientsLIOTHYRONINE SODIUM (25 ug/1)
Marketing started20210201
Package count2

External sources

Source: openFDA. Public-domain (CC0).