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
- 37808-126_a08f35dd-f3d5-5689-c975-0ed213c90c7d
- Product NDC
- 37808-126
- Form
- TABLET, COATED
- Composition / generic term
- levocetirizine dihydrochloride
- Labeler
- HEB
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190615
- Source listing expiry
- 20271231
Source-listed ingredients
- LEVOCETIRIZINE DIHYDROCHLORIDE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 2 BLISTER PACK in 1 BLISTER PACK (37808-126-10) / 5 TABLET, COATED in 1 BLISTER PACK · 37808-126-10
- 1 BOTTLE in 1 BOTTLE (37808-126-35) / 35 TABLET, COATED in 1 BOTTLE · 37808-126-35
- 1 BOTTLE in 1 CARTON (37808-126-80) / 80 TABLET, COATED in 1 BOTTLE · 37808-126-80
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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