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Flecainide Acetate

NDC 72789-383, flecainide acetate, tablet, from PD-Rx Pharmaceuticals, Inc..

Product NDC
72789-383
Status
Listed
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210683
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72789-383 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FLECAINIDE ACETATE100 mg/1

Pharmacologic classes

Antiarrhythmic [EPC]

Package NDCNDC-11Package
72789-383-0172789038301100 TABLET in 1 BOTTLE, PLASTIC (72789-383-01)
72789-383-607278903836060 TABLET in 1 BOTTLE, PLASTIC (72789-383-60)
72789-383-9372789038393180 TABLET in 1 BOTTLE, PLASTIC (72789-383-93)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/abcb261b-30ae-4eb1-baf0-e9667a2bd8cf

Use it

Look up 72789-383 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72789-383 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72789-383. 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.