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MECLIZINE HYDROCHLORIDE

NDC 72189-302, MECLIZINE HYDROCHLORIDE, tablet, from DirectRx.

Product NDC
72189-302
Status
Listed
Labeler
DirectRx
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/72189-302 \
  -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
72189-302-307218903023030 TABLET in 1 BOTTLE (72189-302-30)
72189-302-607218903026060 TABLET in 1 BOTTLE (72189-302-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d27fe828-4fee-3ba9-e053-2995a90ae7b6

Use it

Look up 72189-302 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72189-302 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72189-302. 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.