# spironolactone

NDC: 31722-691
Generic name: spironolactone
Labeler / Manufacturer: Camber Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SUSPENSION
Routes: ORAL
Marketing started: 20250221

FDA application: ANDA218085

## Active ingredients

- SPIRONOLACTONE: 25 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"31722-691"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-691
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4ac2926a-949a-4383-b0b0-92c0822dfcda