United States · FDA National Drug Code directory

HYDROXYZINE HYDROCHLORIDE

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
82804-288_ca843456-0c93-41e8-9bbc-9cd92447f092
Product NDC
82804-288
Form
TABLET, FILM COATED
Composition / generic term
hydroxyzine hydrochloride
Labeler
Proficient Rx LP
Marketing category
ANDA
Marketing start / end (source format)
20230822
Source listing expiry
20271231

Source-listed ingredients

  • HYDROXYZINE DIHYDROCHLORIDE — 10 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET, FILM COATED in 1 BOTTLE (82804-288-30) · 82804-288-30

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →
HYDROXYZINE HYDROCHLORIDE — United States | Molindra Medicines