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Meclizine Hydrochloride

NDC 76420-797, Meclizine Hydrochloride, tablet, from Asclemed USA, Inc..

Product NDC
76420-797
Status
Listed
Labeler
Asclemed USA, Inc.
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/76420-797 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MECLIZINE HYDROCHLORIDE12.5 mg/1

Pharmacologic classes

Antiemetic [EPC]; Emesis Suppression [PE]

Package NDCNDC-11Package
76420-797-0176420079701100 TABLET in 1 BOTTLE (76420-797-01)
76420-797-307642007973030 TABLET in 1 BOTTLE (76420-797-30)
76420-797-607642007976060 TABLET in 1 BOTTLE (76420-797-60)
76420-797-907642007979090 TABLET in 1 BOTTLE (76420-797-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e6a5df4b-5cbf-4a0c-b38a-f4509c9c17db

Use it

Look up 76420-797 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/76420-797 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 76420-797. 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.