# Digoxin

NDC: 57664-437
Generic name: Digoxin
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20150217

FDA application: ANDA076363

## Active ingredients

- DIGOXIN: 125 ug/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"57664-437"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=57664-437
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=62795623-a2bc-4dd2-8989-3b9782bfd80e