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Mexiletine Hydrochloride

NDC 0093-8739, Mexiletine Hydrochloride, capsule, from Teva Pharmaceuticals USA, Inc..

Product NDC
0093-8739
Status
Listed
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA074377
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0093-8739 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MEXILETINE HYDROCHLORIDE150 mg/1

Pharmacologic classes

Antiarrhythmic [EPC]

Package NDCNDC-11Package
0093-8739-0100093873901100 CAPSULE in 1 BOTTLE (0093-8739-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/693da40b-26d4-40d6-87d1-158e256f40ab

  • NADAC price for package 00093873901

    GET /v1/drugs/nadac/00093873901

Use it

Look up 0093-8739 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0093-8739 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0093-8739. 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.