United States · FDA National Drug Code directory
Zyrtec Allergy
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
- 85237-2960_568960cf-2c90-f1b0-e063-6294a90aebc7
- Product NDC
- 85237-2960
- Form
- TABLET, FILM COATED
- Composition / generic term
- Cetirizine Hydrochloride
- Labeler
- Select Consumer Group
- Marketing category
- NDA
- Marketing start / end (source format)
- 20080101
- Source listing expiry
- 20271231
Source-listed ingredients
- CETIRIZINE HYDROCHLORIDE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 POUCH in 1 BLISTER PACK (85237-2960-1) / 1 TABLET, FILM COATED in 1 POUCH (85237-2960-0) · 85237-2960-1
- 20 POUCH in 1 CARTON (85237-2960-3) / 1 TABLET, FILM COATED in 1 POUCH (85237-2960-0) · 85237-2960-3
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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