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Meclizine Hydrochloride

NDC 16571-660, Meclizine Hydrochloride, tablet, from Rising Pharma Holdings, Inc..

Product NDC
16571-660
Status
Listed
Labeler
Rising Pharma Holdings, 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/16571-660 \
  -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
16571-660-0116571066001100 TABLET in 1 BOTTLE (16571-660-01)
16571-660-5016571066050500 TABLET in 1 BOTTLE (16571-660-50)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c9ddc39c-bc6b-42f1-8c5f-5aff2d79c4bd

  • NADAC price for package 16571066001

    GET /v1/drugs/nadac/16571066001

  • NADAC price for package 16571066050

    GET /v1/drugs/nadac/16571066050

Use it

Look up 16571-660 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/16571-660 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 16571-660. 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.