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Hydroxyzine Hydrochloride

NDC 31722-501, Hydroxyzine Hydrochloride, tablet, film coated, from Camber Pharmaceuticals, Inc..

Product NDC
31722-501
Status
Listed
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040805
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/31722-501 \
  -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
31722-501-0131722050101100 TABLET, FILM COATED in 1 BOTTLE (31722-501-01)
31722-501-0531722050105500 TABLET, FILM COATED in 1 BOTTLE (31722-501-05)
31722-501-10317220501101000 TABLET, FILM COATED in 1 BOTTLE (31722-501-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f7e527fe-2f67-45ad-a3ec-146ead819514

Use it

Look up 31722-501 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/31722-501 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 31722-501. 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.