# SPIRONOLACTONE

NDC: 63629-5341
Generic name: SPIRONOLACTONE
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 19860723

FDA application: ANDA089424

## Active ingredients

- SPIRONOLACTONE: 50 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63629-5341"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63629-5341
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cae68fd6-5161-4650-bcde-6db98cbe6c8b