United States · FDA National Drug Code directory
Cetirizine Hydrochloride (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
- 69842-237_621f3d87-d69e-41e6-8ece-22099cb87c01
- Product NDC
- 69842-237
- Form
- TABLET
- Composition / generic term
- Cetirizine Hydrochloride
- Labeler
- CVS Pharmacy, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190726
- Source listing expiry
- 20261231
Source-listed ingredients
- CETIRIZINE HYDROCHLORIDE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BLISTER PACK in 1 CARTON (69842-237-01) / 14 TABLET in 1 BLISTER PACK · 69842-237-01
- 1 BOTTLE in 1 CARTON (69842-237-09) / 30 TABLET in 1 BOTTLE · 69842-237-09
- 1 BOTTLE in 1 CARTON (69842-237-17) / 45 TABLET in 1 BOTTLE · 69842-237-17
- 1 BOTTLE in 1 CARTON (69842-237-19) / 90 TABLET in 1 BOTTLE · 69842-237-19
- 1 BOTTLE in 1 CARTON (69842-237-23) / 120 TABLET in 1 BOTTLE · 69842-237-23
- 365 TABLET in 1 BOTTLE (69842-237-39) · 69842-237-39
- 2 BOTTLE in 1 CARTON (69842-237-45) / 120 TABLET in 1 BOTTLE · 69842-237-45
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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