# SPIRONOLACTONE

NDC: 53489-329
Generic name: SPIRONOLACTONE
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
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: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"53489-329"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=53489-329
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c23b6b9b-aec3-48a8-a518-76e4097f6479