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
- 72789-216_3caab728-dec4-fe78-e063-6294a90a17ec
- Product NDC
- 72789-216
- Form
- TABLET, FILM COATED
- Composition / generic term
- Hydroxyzine Hydrochloride
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20121009
- Source listing expiry
- 20261231
Source-listed ingredients
- HYDROXYZINE DIHYDROCHLORIDE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-216-04) · 72789-216-04
- 12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-216-12) · 72789-216-12
- 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-216-20) · 72789-216-20
- 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-216-30) · 72789-216-30
- 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-216-40) · 72789-216-40
- 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-216-60) · 72789-216-60
- 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-216-90) · 72789-216-90
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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