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
- 71335-2283_126ac3f1-d0d2-4166-9727-a13d3f728447
- Product NDC
- 71335-2283
- Form
- TABLET
- Composition / generic term
- levocetirizine dihydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140909
- Source listing expiry
- 20271231
Source-listed ingredients
- LEVOCETIRIZINE DIHYDROCHLORIDE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 TABLET in 1 BOTTLE (71335-2283-1) · 71335-2283-1
- 35 TABLET in 1 BOTTLE (71335-2283-2) · 71335-2283-2
- 5 TABLET in 1 BOTTLE (71335-2283-3) · 71335-2283-3
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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