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PROPAFENONE HYDROCHLORIDE

NDC 16571-736, PROPAFENONE HYDROCHLORIDE, capsule, extended release, from Rising Pharma Holdings, Inc..

Product NDC
16571-736
Status
Listed
Labeler
Rising Pharma Holdings, Inc.
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA205956
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/16571-736 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PROPAFENONE HYDROCHLORIDE225 mg/1

Pharmacologic classes

Antiarrhythmic [EPC]

Package NDCNDC-11Package
16571-736-061657107360660 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (16571-736-06)
16571-736-5016571073650500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (16571-736-50)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/36cf4555-6fe9-42d8-8d3b-3ca9c134a5b8

  • NADAC price for package 16571073606

    GET /v1/drugs/nadac/16571073606

Use it

Look up 16571-736 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/16571-736 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 16571-736. 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.