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Meclizine Hydrochloride

NDC 76420-798, Meclizine Hydrochloride, tablet, from Asclemed USA, Inc..

Product NDC
76420-798
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/76420-798 \
  -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
76420-798-0176420079801100 TABLET in 1 BOTTLE (76420-798-01)
76420-798-307642007983030 TABLET in 1 BOTTLE (76420-798-30)
76420-798-607642007986060 TABLET in 1 BOTTLE (76420-798-60)
76420-798-907642007989090 TABLET in 1 BOTTLE (76420-798-90)

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 76420-798 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/76420-798 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 76420-798. 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.