FDA NDC
GAVILYTE-N
This name is from the loaded FDA file.
Source: FDA NDC Directory, live from openFDA. Publisher page
- NDC
- 43386-050
- Proprietary name
- GAVILYTE-N
- Nonproprietary name
- polyethylene glycol-3350, sodium chloride, potassium chloride and sodium bicarbonate
- Labeler
- Lupin Pharmaceuticals,Inc.
- Dosage form
- POWDER, FOR SOLUTION
- Strength
- 420 g/438.4g
Run it in Rivvi
Which 2027 plans near you dropped or restricted polyethylene glycol-3350, sodium chloride, potassium chloride and sodium bicarbonate?
Tier changes and new prior auth, step therapy or quantity limits, plan by plan, from the CMS Part D files.
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