United States · FDA National Drug Code directory
Amiodarone Hydrochloride
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
- 51672-4025_4cc4c3cb-aced-a125-e063-6394a90aee93
- Product NDC
- 51672-4025
- Form
- TABLET
- Composition / generic term
- Amiodarone Hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20010330
- Source listing expiry
- 20271231
Source-listed ingredients
- AMIODARONE HYDROCHLORIDE — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 500 TABLET in 1 BOTTLE (51672-4025-2) · 51672-4025-2
- 1000 TABLET in 1 BOTTLE (51672-4025-3) · 51672-4025-3
- 60 TABLET in 1 BOTTLE (51672-4025-4) · 51672-4025-4
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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