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Levothyroxine sodium

NDC 68071-2531 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameLevothyroxine Sodium
Labeler / ManufacturerNuCare Pharmaceuticals,Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA212399
Dosage form / routeTABLET · ORAL
Active ingredientsLEVOTHYROXINE SODIUM (125 ug/1)
Marketing started20201203
Package count1

External sources

Source: openFDA. Public-domain (CC0).