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Meclizine Hydrochloride

NDC 71205-786, Meclizine Hydrochloride, tablet, from Proficient Rx LP.

Product NDC
71205-786
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/71205-786 \
  -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
71205-786-107120507861010 TABLET in 1 BOTTLE (71205-786-10)
71205-786-207120507862020 TABLET in 1 BOTTLE (71205-786-20)
71205-786-307120507863030 TABLET in 1 BOTTLE (71205-786-30)
71205-786-607120507866060 TABLET in 1 BOTTLE (71205-786-60)
71205-786-907120507869090 TABLET in 1 BOTTLE (71205-786-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b91435d1-fb95-4939-8478-84e41f44f732

Use it

Look up 71205-786 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-786 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-786. 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.