# SPIRONOLACTONE

NDC: 71335-2366
Generic name: SPIRONOLACTONE
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19860723

FDA application: ANDA089424

## Active ingredients

- SPIRONOLACTONE: 25 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71335-2366"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71335-2366
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ca194a2a-ed16-40f6-a78c-45c5f3392170