FDA NDC Directory · JSON-LD · Markdown

Levothyroxine sodium

NDC 68788-8792 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA207588
Dosage form / routeTABLET · ORAL
Active ingredientsLEVOTHYROXINE SODIUM (88 ug/1)
Marketing started20241217
Package count3

External sources

Source: openFDA. Public-domain (CC0).