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
- 29300-359_ca43a6d6-5537-4881-bf75-b43ade430dd1
- Product NDC
- 29300-359
- Form
- TABLET
- Composition / generic term
- Amiodarone Hydrochloride
- Labeler
- Unichem Pharmaceuticals (USA), Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200901
- Source listing expiry
- 20261231
Source-listed ingredients
- AMIODARONE HYDROCHLORIDE — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 500 TABLET in 1 BOTTLE (29300-359-05) · 29300-359-05
- 60 TABLET in 1 BOTTLE (29300-359-16) · 29300-359-16
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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