United States · FDA National Drug Code directory
Levocetirizine Dihydrochloride
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
- 69230-321_7ca0cee0-b628-4266-b361-ad5c52b6f11e
- Product NDC
- 69230-321
- Form
- TABLET, FILM COATED
- Composition / generic term
- Levocetirizine Dihydrochloride
- Labeler
- Camber Consumer Care Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20201028
- Source listing expiry
- 20261231
Source-listed ingredients
- LEVOCETIRIZINE DIHYDROCHLORIDE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 BLISTER PACK in 1 CARTON (69230-321-01) / 10 TABLET, FILM COATED in 1 BLISTER PACK · 69230-321-01
- 1000 TABLET, FILM COATED in 1 BOTTLE (69230-321-10) · 69230-321-10
- 1 BOTTLE in 1 CARTON (69230-321-31) / 35 TABLET, FILM COATED in 1 BOTTLE · 69230-321-31
- 1 BOTTLE in 1 CARTON (69230-321-32) / 55 TABLET, FILM COATED in 1 BOTTLE · 69230-321-32
- 1 BOTTLE in 1 CARTON (69230-321-33) / 80 TABLET, FILM COATED in 1 BOTTLE · 69230-321-33
- 1 BOTTLE in 1 CARTON (69230-321-34) / 180 TABLET, FILM COATED in 1 BOTTLE · 69230-321-34
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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