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MECLIZINE HYDROCHLORIDE

NDC 71335-3141, MECLIZINE, tablet, from Bryant Ranch Prepack.

Product NDC
71335-3141
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202640
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-3141 \
  -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
71335-3141-17133531410130 TABLET in 1 BOTTLE (71335-3141-1)
71335-3141-27133531410260 TABLET in 1 BOTTLE (71335-3141-2)
71335-3141-37133531410390 TABLET in 1 BOTTLE (71335-3141-3)
71335-3141-47133531410428 TABLET in 1 BOTTLE (71335-3141-4)
71335-3141-57133531410520 TABLET in 1 BOTTLE (71335-3141-5)
71335-3141-671335314106120 TABLET in 1 BOTTLE (71335-3141-6)
71335-3141-771335314107100 TABLET in 1 BOTTLE (71335-3141-7)
71335-3141-87133531410810 TABLET in 1 BOTTLE (71335-3141-8)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1079db3f-d8ad-4c25-aa91-8ac8054ee4f2

Use it

Look up 71335-3141 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-3141 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-3141. 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.