FDA NDC Directory · JSON-LD · Markdown

Levothyroxine sodium

NDC 68788-7954 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameLevothyroxine Sodium
Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA212399
Dosage form / routeTABLET · ORAL
Active ingredientsLEVOTHYROXINE SODIUM (75 ug/1)
Marketing started20210709
Package count2

External sources

Source: openFDA. Public-domain (CC0).