United States · FDA National Drug Code directory

LANOXIN

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
71610-019_1d7755ac-5480-4614-bc20-beb024ab95f2
Product NDC
71610-019
Form
TABLET
Composition / generic term
digoxin
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Marketing category
NDA
Marketing start / end (source format)
20120930
Source listing expiry
20261231

Source-listed ingredients

  • DIGOXIN — .125 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 90 TABLET in 1 BOTTLE (71610-019-60) · 71610-019-60

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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