# Spironolactone

NDC: 68788-8452
Generic name: Spironolactone
Labeler / Manufacturer: Preferred Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20230530

FDA application: ANDA040750

## Active ingredients

- SPIRONOLACTONE: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68788-8452"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-8452
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5e456f3c-f93e-41c6-80c5-a737ed70feda