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Mexiletine Hydrochloride

NDC 33342-556, Mexiletine Hydrochloride, capsule, from Macleods Pharmaceuticals Limited.

Product NDC
33342-556
Status
Listed
Labeler
Macleods Pharmaceuticals Limited
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA219987
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/33342-556 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MEXILETINE HYDROCHLORIDE200 mg/1

Pharmacologic classes

Antiarrhythmic [EPC]

Package NDCNDC-11Package
33342-556-1133342055611100 CAPSULE in 1 CONTAINER (33342-556-11)
33342-556-123334205561210 BLISTER PACK in 1 CARTON (33342-556-12) / 10 CAPSULE in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a61a07f6-0b48-4dcd-ad42-5d90f6e69ab1

Use it

Look up 33342-556 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/33342-556 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 33342-556. 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.