FDA NDC

Duramorph

This name is from the loaded FDA file.

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

NDC
0641-6020
Proprietary name
Duramorph
Nonproprietary name
morphine sulfate
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
INJECTION
Strength
.5 mg/mL

Run it in Rivvi

Which 2027 plans near you dropped or restricted morphine sulfate?

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.