FDA NDC
Spironolactone and Hydrochlorothiazide
This name is from the loaded FDA file.
Source: FDA NDC Directory, live from openFDA. Publisher page
- NDC
- 66993-188
- Proprietary name
- Spironolactone and Hydrochlorothiazide
- Nonproprietary name
- spironolactone and hydrochlorothiazide
- Labeler
- Prasco Laboratories
- Dosage form
- TABLET, FILM COATED
- Strength
- 25 mg/1
Run it in Rivvi
Which 2027 plans near you dropped or restricted spironolactone and hydrochlorothiazide?
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.