# Spironolactone

NDC: 43063-832
Generic name: spironolactone
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20170602

FDA application: ANDA203512

## Active ingredients

- SPIRONOLACTONE: 25 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43063-832"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43063-832
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c223a334-7383-429f-b8e3-a21200f16962