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
- 72673-073_487d000e-9dec-3e6f-e063-6294a90ae8b0
- Product NDC
- 72673-073
- Form
- INJECTION, SOLUTION
- Composition / generic term
- amiodarone hydrochloride
- Labeler
- Zhejiang Poly Pharm. Co., Ltd.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230206
- Source listing expiry
- 20271231
Source-listed ingredients
- AMIODARONE HYDROCHLORIDE — 50 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 18 mL in 1 VIAL, GLASS (72673-073-01) · 72673-073-01
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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