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
- 0115-9822_c02900ce-5cf2-4587-8b64-c65c1a0be303
- Product NDC
- 0115-9822
- Form
- TABLET
- Composition / generic term
- DIGOXIN
- Labeler
- Amneal Pharmaceuticals of New York LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20090720
- Source listing expiry
- 20271231
Source-listed ingredients
- DIGOXIN — 250 ug/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (0115-9822-01) · 0115-9822-01
- 500 TABLET in 1 BOTTLE (0115-9822-02) · 0115-9822-02
- 1000 TABLET in 1 BOTTLE (0115-9822-03) · 0115-9822-03
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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