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Hydroxyzine Hydrochloride

NDC 65162-671, Hydroxyzine, tablet, film coated, from Amneal Pharmaceuticals LLC.

Product NDC
65162-671
Status
Listed
Labeler
Amneal Pharmaceuticals LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040808
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65162-671 \
  -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
65162-671-1065162067110100 TABLET, FILM COATED in 1 BOTTLE (65162-671-10)
65162-671-11651620671111000 TABLET, FILM COATED in 1 BOTTLE (65162-671-11)
65162-671-5065162067150500 TABLET, FILM COATED in 1 BOTTLE (65162-671-50)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/89901966-724b-4773-98b8-ea663ceabd53

Use it

Look up 65162-671 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65162-671 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65162-671. 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.