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MECLIZINE HYDROCHLORIDE

NDC 76420-130, Meclizine Hydrocloride, tablet, from Asclemed USA, Inc..

Product NDC
76420-130
Status
Listed
Labeler
Asclemed USA, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040659
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/76420-130 \
  -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
76420-130-107642001301010 TABLET in 1 BOTTLE (76420-130-10)
76420-130-207642001302020 TABLET in 1 BOTTLE (76420-130-20)
76420-130-307642001303030 TABLET in 1 BOTTLE (76420-130-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5c70e61b-a1e6-4981-92e2-1050cee08baa

Use it

Look up 76420-130 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/76420-130 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 76420-130. 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.