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
- 63629-4929_9efda664-6143-4427-9290-60c6abf0ec0b
- Product NDC
- 63629-4929
- Form
- TABLET, FILM COATED
- Composition / generic term
- Hydroxyzine hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140820
- Source listing expiry
- 20261231
Source-listed ingredients
- HYDROXYZINE DIHYDROCHLORIDE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 120 TABLET, FILM COATED in 1 BOTTLE (63629-4929-1) · 63629-4929-1
- 20 TABLET, FILM COATED in 1 BOTTLE (63629-4929-2) · 63629-4929-2
- 30 TABLET, FILM COATED in 1 BOTTLE (63629-4929-3) · 63629-4929-3
- 60 TABLET, FILM COATED in 1 BOTTLE (63629-4929-4) · 63629-4929-4
- 90 TABLET, FILM COATED in 1 BOTTLE (63629-4929-5) · 63629-4929-5
Source and coverage
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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.
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