FDA NDC

Levothyroxine Sodium

This name is from the loaded FDA file.

Source: FDA NDC Directory, live from openFDA. Publisher page

NDC
63323-649
Proprietary name
Levothyroxine Sodium
Nonproprietary name
LEVOTHYROXINE SODIUM ANHYDROUS
Labeler
Fresenius Kabi USA, LLC
Dosage form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Strength
100 ug/5mL

Run it in Rivvi

Which 2027 plans near you dropped or restricted LEVOTHYROXINE SODIUM ANHYDROUS?

Tier changes and new prior auth, step therapy or quantity limits, plan by plan, from the CMS Part D files.

Free to start. Opens Rivvi, the AI workspace for healthcare teams.

Try it on your own data today.

Free to start. Most teams are using it the same day.