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HYDROXYZINE HYDROCHLORIDE

NDC 11534-205, hydroxyzine hydrochloride, tablet, film coated, from Sunrise Pharmaceutical, Inc..

Product NDC
11534-205
Status
Listed
Labeler
Sunrise Pharmaceutical, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207121
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/11534-205 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HYDROXYZINE DIHYDROCHLORIDE25 mg/1

Pharmacologic classes

Antihistamine [EPC]; Histamine Receptor Antagonists [MoA]

Package NDCNDC-11Package
11534-205-0111534020501100 TABLET, FILM COATED in 1 BOTTLE (11534-205-01)
11534-205-03115340205031000 TABLET, FILM COATED in 1 BOTTLE (11534-205-03)
11534-205-0411534020504500 TABLET, FILM COATED in 1 BOTTLE (11534-205-04)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/94561525-a565-4193-b64d-e1459ab05678

Use it

Look up 11534-205 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/11534-205 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 11534-205. 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.