United States · FDA National Drug Code directory
Cetirizine 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
- 51672-2106_5698bba4-d090-a558-e063-6294a90a600a
- Product NDC
- 51672-2106
- Form
- SOLUTION
- Composition / generic term
- Cetirizine Hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20110520
- Source listing expiry
- 20271231
Source-listed ingredients
- CETIRIZINE HYDROCHLORIDE — 1 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (51672-2106-1) / 240 mL in 1 BOTTLE · 51672-2106-1
- 1 BOTTLE in 1 CARTON (51672-2106-4) / 60 mL in 1 BOTTLE · 51672-2106-4
- 1 BOTTLE in 1 CARTON (51672-2106-8) / 120 mL in 1 BOTTLE · 51672-2106-8
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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