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Meclizine Hydrochloride

NDC 68071-3748, Meclizine Hydrochloride, tablet, from NuCare Pharmaceuticals, Inc..

Product NDC
68071-3748
Status
Listed
Labeler
NuCare Pharmaceuticals, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213957
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68071-3748 \
  -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
68071-3748-4680713748044 TABLET in 1 BOTTLE (68071-3748-4)
68071-3748-6680713748066 TABLET in 1 BOTTLE (68071-3748-6)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2990e296-2d60-70c0-e063-6394a90abbe4

Use it

Look up 68071-3748 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68071-3748 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68071-3748. 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.