FDA NDC
ciprofloxacin hydrochloride and hydrocortisone
This name is from the loaded FDA file.
Source: FDA NDC Directory, live from openFDA. Publisher page
- NDC
- 0781-6218
- Proprietary name
- ciprofloxacin hydrochloride and hydrocortisone
- Nonproprietary name
- ciprofloxacin hydrochloride and hydrocortisone
- Labeler
- Sandoz Inc
- Dosage form
- SUSPENSION/ DROPS
- Strength
- 2 mg/mL
Run it in Rivvi
Which 2027 plans near you dropped or restricted ciprofloxacin hydrochloride and hydrocortisone?
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.