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Meclizine Hydrochloride

NDC 70518-3768, Meclizine Hydrochloride, tablet, from REMEDYREPACK INC..

Product NDC
70518-3768
Status
Listed
Labeler
REMEDYREPACK 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/70518-3768 \
  -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
70518-3768-07051837680030 TABLET in 1 BOTTLE, PLASTIC (70518-3768-0)
70518-3768-17051837680190 TABLET in 1 BOTTLE, PLASTIC (70518-3768-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d53bf04e-5cfc-4974-9b24-2cce545d1bd0

Use it

Look up 70518-3768 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3768 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-3768. 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.