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Amiodarone Hydrochloride

NDC 51672-4056, Amiodarone Hydrochloride, tablet, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-4056
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076362
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4056 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • AMIODARONE HYDROCHLORIDE300 mg/1

Pharmacologic classes

Antiarrhythmic [EPC]; Cytochrome P450 1A2 Inhibitors [MoA]; Cytochrome P450 2C9 Inhibitors [MoA]; Cytochrome P450 2D6 Inhibitors [MoA]; Cytochrome P450 3A Inhibitors [MoA]; P-Glycoprotein Inhibitors [MoA]

Package NDCNDC-11Package
51672-4056-151672405601100 TABLET in 1 BOTTLE (51672-4056-1)
51672-4056-3516724056031000 TABLET in 1 BOTTLE (51672-4056-3)
51672-4056-65167240560630 TABLET in 1 BOTTLE (51672-4056-6)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7ccd3733-c3af-4a11-8500-0f99194c1472

Use it

Look up 51672-4056 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4056 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-4056. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.