United States · FDA National Drug Code directory
Cetirizine Hydrochloride 10 mg
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
- 10267-3579_3633ac85-4814-e6a7-e063-6294a90a375d
- Product NDC
- 10267-3579
- Form
- TABLET, FILM COATED
- Composition / generic term
- Cetirizine Hydrochloride 10 mg
- Labeler
- Contract Pharmacal Corp.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250416
- Source listing expiry
- 20261231
Source-listed ingredients
- CETIRIZINE HYDROCHLORIDE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (10267-3579-1) / 100 TABLET, FILM COATED in 1 BOTTLE · 10267-3579-1
- 1 BOTTLE in 1 CARTON (10267-3579-3) / 30 TABLET, FILM COATED in 1 BOTTLE · 10267-3579-3
- 100 TABLET, FILM COATED in 1 BOTTLE (10267-3579-4) · 10267-3579-4
- 365 TABLET, FILM COATED in 1 BOTTLE (10267-3579-6) · 10267-3579-6
- 1 BOTTLE in 1 CARTON (10267-3579-7) / 60 TABLET, FILM COATED in 1 BOTTLE · 10267-3579-7
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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