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Meclizine Hydrochloride

NDC 67046-0869, Meclizine Hydrochloride, tablet, from Coupler LLC.

Product NDC
67046-0869
Status
Listed
Labeler
Coupler LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA010721
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/67046-0869 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MECLIZINE HYDROCHLORIDE25 mg/1

Pharmacologic classes

Antiemetic [EPC]; Emesis Suppression [PE]

Package NDCNDC-11Package
67046-0869-36704608690330 TABLET in 1 BLISTER PACK (67046-0869-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/598eb392-1dfe-c08c-e063-6394a90a4c7d

Use it

Look up 67046-0869 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/67046-0869 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 67046-0869. 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.