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
- 71335-3088_8db62cda-c456-47b3-85bb-b67f777c0a9a
- Product NDC
- 71335-3088
- Form
- TABLET, FILM COATED
- Composition / generic term
- Hydroxyzine Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20211007
- 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 (71335-3088-1) · 71335-3088-1
- 100 TABLET, FILM COATED in 1 BOTTLE (71335-3088-2) · 71335-3088-2
- 20 TABLET, FILM COATED in 1 BOTTLE (71335-3088-3) · 71335-3088-3
- 90 TABLET, FILM COATED in 1 BOTTLE (71335-3088-4) · 71335-3088-4
- 15 TABLET, FILM COATED in 1 BOTTLE (71335-3088-5) · 71335-3088-5
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-3088-6) · 71335-3088-6
- 120 TABLET, FILM COATED in 1 BOTTLE (71335-3088-7) · 71335-3088-7
- 10 TABLET, FILM COATED in 1 BOTTLE (71335-3088-8) · 71335-3088-8
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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