United States · FDA National Drug Code directory
allergy relief
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
- 37808-583_e2ba6632-3350-4d5f-a03e-5e68dce98576
- Product NDC
- 37808-583
- Form
- TABLET, FILM COATED
- Composition / generic term
- Cetirizine Hydrochloride
- Labeler
- H E B
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180126
- Source listing expiry
- 20271231
Source-listed ingredients
- CETIRIZINE HYDROCHLORIDE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (37808-583-06) / 70 TABLET, FILM COATED in 1 BOTTLE · 37808-583-06
- 1 BOTTLE in 1 CARTON (37808-583-39) / 30 TABLET, FILM COATED in 1 BOTTLE · 37808-583-39
- 14 BLISTER PACK in 1 CARTON (37808-583-66) / 1 TABLET, FILM COATED in 1 BLISTER PACK · 37808-583-66
- 1 BOTTLE in 1 CARTON (37808-583-76) / 120 TABLET, FILM COATED in 1 BOTTLE · 37808-583-76
- 1 BOTTLE in 1 CARTON (37808-583-87) / 300 TABLET, FILM COATED in 1 BOTTLE (37808-583-00) · 37808-583-87
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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