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
- 0517-4201_83de333d-1bf1-4168-8614-6bc79c26d5d0
- Product NDC
- 0517-4201
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Hydroxyzine Hydrochloride
- Labeler
- American Regent, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19900930
- Source listing expiry
- 20261231
Source-listed ingredients
- HYDROXYZINE DIHYDROCHLORIDE — 25 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-4201-25) / 1 mL in 1 VIAL, SINGLE-DOSE (0517-4201-01) · 0517-4201-25
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 →