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Meclizine Hydrochloride

NDC 68071-2380, Meclizine Hydrochloride, tablet, from NuCare Pharmaceuticals,Inc..

Product NDC
68071-2380
Status
Listed
Labeler
NuCare Pharmaceuticals,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/68071-2380 \
  -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
68071-2380-26807123800220 TABLET in 1 BOTTLE (68071-2380-2)
68071-2380-36807123800330 TABLET in 1 BOTTLE (68071-2380-3)
68071-2380-96807123800990 TABLET in 1 BOTTLE (68071-2380-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/beb36d86-9fb7-1f60-e053-2995a90aac13

Use it

Look up 68071-2380 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68071-2380 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68071-2380. 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.