FDA NDC
Goprelto
This name is from the loaded FDA file.
Source: FDA NDC Directory, live from openFDA. Publisher page
- NDC
- 70839-359
- Proprietary name
- Goprelto
- Nonproprietary name
- cocaine hydrochloride
- Labeler
- LXO US Inc.
- Dosage form
- SOLUTION
- Strength
- 40 mg/mL
Run it in Rivvi
Which 2027 plans near you dropped or restricted cocaine hydrochloride?
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.