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Hydroxyzine Hydrochloride

NDC 71335-3034, Hydroxyzine Hydrochloride, tablet, film coated, from Bryant Ranch Prepack.

Product NDC
71335-3034
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA087871
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-3034 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HYDROXYZINE DIHYDROCHLORIDE10 mg/1

Pharmacologic classes

Antihistamine [EPC]; Histamine Receptor Antagonists [MoA]

Package NDCNDC-11Package
71335-3034-171335303401500 TABLET, FILM COATED in 1 BOTTLE (71335-3034-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9504897e-febc-4293-a2dc-9f79f55ea821

Use it

Look up 71335-3034 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-3034 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-3034. 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.