# SPIRONOLACTONE

NDC: 68071-3795
Generic name: SPIRONOLACTONE
Labeler / Manufacturer: NuCare Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20191213

FDA application: ANDA202187

## Active ingredients

- SPIRONOLACTONE: 50 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68071-3795"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68071-3795
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2e5e782d-9ceb-d4a4-e063-6294a90aba3a