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MECLIZINE HYDROCHLORIDE

NDC 23155-943, MECLIZINE, tablet, from Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc..

Product NDC
23155-943
Status
Listed
Labeler
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA205136
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/23155-943 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MECLIZINE HYDROCHLORIDE50 mg/1

Pharmacologic classes

Antiemetic [EPC]; Emesis Suppression [PE]

Package NDCNDC-11Package
23155-943-0123155094301100 TABLET in 1 BOTTLE (23155-943-01)
23155-943-10231550943101000 TABLET in 1 PACKAGE (23155-943-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b11c10b9-f40e-4ea7-9c5d-118517049f9d

  • NADAC price for package 23155094301

    GET /v1/drugs/nadac/23155094301

Use it

Look up 23155-943 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/23155-943 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 23155-943. 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.