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MEXILETINE HYDROCHLORIDE

NDC 82012-027, mexiletine hydrochloride, capsule, from Senores Pharmaceuticals, Inc..

Product NDC
82012-027
Status
Listed
Labeler
Senores Pharmaceuticals, Inc.
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202111
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/82012-027 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MEXILETINE HYDROCHLORIDE150 mg/1

Pharmacologic classes

Antiarrhythmic [EPC]

Package NDCNDC-11Package
82012-027-0482012002704100 CAPSULE in 1 BOTTLE (82012-027-04)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c4a60f9e-fed1-4172-adc4-0be84ac65db9

Use it

Look up 82012-027 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/82012-027 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 82012-027. 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.