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MEXILETINE HYDROCHLORIDE

NDC 62756-956, mexiletine hydrochloride, capsule, from Sun Pharmaceutical Industries, Inc..

Product NDC
62756-956
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214089
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/62756-956 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MEXILETINE HYDROCHLORIDE200 mg/1

Pharmacologic classes

Antiarrhythmic [EPC]

Package NDCNDC-11Package
62756-956-0162756095601100 CAPSULE in 1 BOTTLE (62756-956-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2d0c61ca-4c99-42f9-8f00-e0e9d2672a39

  • NADAC price for package 62756095601

    GET /v1/drugs/nadac/62756095601

Use it

Look up 62756-956 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62756-956 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62756-956. 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.