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
- 16714-082_1a8febc0-9d51-4026-8ea6-6cba69e841c5
- Product NDC
- 16714-082
- Form
- TABLET
- Composition / generic term
- HydrOXYzine Hydrochloride
- Labeler
- Northstar RxLLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20091111
- Source listing expiry
- 20271231
Source-listed ingredients
- HYDROXYZINE DIHYDROCHLORIDE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (16714-082-10) · 16714-082-10
- 500 TABLET in 1 BOTTLE (16714-082-11) · 16714-082-11
- 1000 TABLET in 1 BOTTLE (16714-082-12) · 16714-082-12
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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