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Hydroxyzine Hydrochloride

NDC 10702-012, Hydroxyzine Hydrochloride, tablet, film coated, from KVK-Tech, Inc..

Product NDC
10702-012
Status
Listed
Labeler
KVK-Tech, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040786
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/10702-012 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HYDROXYZINE DIHYDROCHLORIDE50 mg/1

Pharmacologic classes

Antihistamine [EPC]; Histamine Receptor Antagonists [MoA]

Package NDCNDC-11Package
10702-012-0110702001201100 TABLET, FILM COATED in 1 BOTTLE (10702-012-01)
10702-012-10107020012101000 TABLET, FILM COATED in 1 BOTTLE (10702-012-10)
10702-012-5010702001250500 TABLET, FILM COATED in 1 BOTTLE (10702-012-50)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/adc4cb73-77c6-48ff-aaf2-b3568d53de1f

Use it

Look up 10702-012 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/10702-012 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 10702-012. 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.