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
- 58602-444_09cf1596-6539-44ff-9f90-a0fb1f218b4e
- Product NDC
- 58602-444
- Form
- TABLET
- Composition / generic term
- Cetirizine Hydrochloride
- Labeler
- Aurohealth LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20150805
- Source listing expiry
- 20271231
Source-listed ingredients
- CETIRIZINE HYDROCHLORIDE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (58602-444-09) / 30 TABLET in 1 BOTTLE · 58602-444-09
- 1 BOTTLE in 1 CARTON (58602-444-17) / 45 TABLET in 1 BOTTLE · 58602-444-17
- 10 BLISTER PACK in 1 CARTON (58602-444-21) / 10 TABLET in 1 BLISTER PACK · 58602-444-21
- 1000 TABLET in 1 BOTTLE (58602-444-41) · 58602-444-41
- 75 TABLET in 1 PACKAGE, COMBINATION (58602-444-47) · 58602-444-47
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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