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Amiodarone Hydrochloride

NDC 70518-3246, Amiodarone Hydrochloride, tablet, from REMEDYREPACK INC..

Product NDC
70518-3246
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213446
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3246 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • AMIODARONE HYDROCHLORIDE200 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
70518-3246-17051832460150 POUCH in 1 BOX (70518-3246-1) / 1 TABLET in 1 POUCH (70518-3246-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4c149392-a4f0-4e2d-a13f-2b94810005de

Use it

Look up 70518-3246 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3246 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-3246. 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.