FDA NDC
OXYBUTYNIN CHLORIDE
This name is from the loaded FDA file.
Source: FDA NDC Directory, live from openFDA. Publisher page
- NDC
- 50090-8078
- Proprietary name
- OXYBUTYNIN CHLORIDE
- Nonproprietary name
- OXYBUTYNIN CHLORIDE
- Labeler
- A-S Medication Solutions
- Dosage form
- TABLET
- Strength
- 5 mg/1
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Which 2027 plans near you dropped or restricted OXYBUTYNIN CHLORIDE?
Tier changes and new prior auth, step therapy or quantity limits, plan by plan, from the CMS Part D files.
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