# Digoxin

NDC: 0904-5921
Generic name: Digoxin
Labeler / Manufacturer: Major Pharmaceuticals
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20090610

FDA application: ANDA077002

## 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:"0904-5921"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0904-5921
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=48cad559-c17b-4d41-a154-e664e958c1c0