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Meclizine Hydrochloride

NDC 71205-647, Meclizine Hydrochloride, tablet, from Proficient Rx LP.

Product NDC
71205-647
Status
Listed
Labeler
Proficient Rx LP
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/71205-647 \
  -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
71205-647-107120506471010 TABLET in 1 BOTTLE (71205-647-10)
71205-647-907120506479090 TABLET in 1 BOTTLE (71205-647-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/92e8390b-5173-4aa1-906d-35d2c0eaaaf6

Use it

Look up 71205-647 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-647 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-647. 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.