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Hydroxyzine Hydrochloride

NDC 72162-1332, Hydroxyzine Hydrochloride, tablet, film coated, from Bryant Ranch Prepack.

Product NDC
72162-1332
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040600
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72162-1332 \
  -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
72162-1332-37216213320330 TABLET, FILM COATED in 1 BOTTLE (72162-1332-3)
72162-1332-97216213320990 TABLET, FILM COATED in 1 BOTTLE (72162-1332-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/dd9e5dc5-720c-4de8-abae-6404c31f341f

Use it

Look up 72162-1332 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72162-1332 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72162-1332. 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.