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Propafenone Hydrochloride

NDC 68382-522, Propafenone Hydrochloride, capsule, extended release, from Zydus Pharmaceuticals (USA) Inc..

Product NDC
68382-522
Status
Listed
Labeler
Zydus Pharmaceuticals (USA) Inc.
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214184
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68382-522 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PROPAFENONE HYDROCHLORIDE225 mg/1

Pharmacologic classes

Antiarrhythmic [EPC]

Package NDCNDC-11Package
68382-522-0568382052205500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-522-05)
68382-522-146838205221460 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-522-14)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/163564b6-a8bf-4258-8ef9-19e33fb2d7bc

Use it

Look up 68382-522 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68382-522 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68382-522. 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.