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Amiodarone Hydrochloride

NDC 51672-4057, Amiodarone Hydrochloride, tablet, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-4057
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/51672-4057 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • AMIODARONE HYDROCHLORIDE400 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
51672-4057-05167240570010 BLISTER PACK in 1 CARTON (51672-4057-0) / 10 TABLET in 1 BLISTER PACK
51672-4057-65167240570630 TABLET in 1 BOTTLE (51672-4057-6)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

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

  • NADAC price for package 51672405706

    GET /v1/drugs/nadac/51672405706

Use it

Look up 51672-4057 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4057 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-4057. 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.