United States · FDA National Drug Code directory
Digoxin
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
- 0781-3059_62ffbb27-b026-4fb2-b2a1-5c170036b8cf
- Product NDC
- 0781-3059
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Digoxin
- Labeler
- Sandoz Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20030821
- Source listing expiry
- 20261231
Source-listed ingredients
- DIGOXIN — 250 ug/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 AMPULE in 1 CARTON (0781-3059-95) / 2 mL in 1 AMPULE (0781-3059-72) · 0781-3059-95
Source and coverage
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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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