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
- 58602-812_09cf1596-6539-44ff-9f90-a0fb1f218b4e
- Product NDC
- 58602-812
- 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 — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 BLISTER PACK in 1 CARTON (58602-812-04) / 10 TABLET in 1 BLISTER PACK (58602-812-83) · 58602-812-04
- 1 BOTTLE in 1 CARTON (58602-812-09) / 30 TABLET in 1 BOTTLE · 58602-812-09
- 1 BOTTLE in 1 CARTON (58602-812-17) / 45 TABLET in 1 BOTTLE · 58602-812-17
- 1 BOTTLE in 1 CARTON (58602-812-23) / 120 TABLET in 1 BOTTLE · 58602-812-23
- 1 BOTTLE in 1 CARTON (58602-812-39) / 365 TABLET in 1 BOTTLE · 58602-812-39
- 1000 TABLET in 1 BOTTLE (58602-812-41) · 58602-812-41
- 75 TABLET in 1 PACKAGE, COMBINATION (58602-812-99) · 58602-812-99
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →