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
41250-488_c58b2c75-6d42-41e4-a4e2-7d59c356a92d
Product NDC
41250-488
Form
TABLET, FILM COATED
Composition / generic term
levocetirizine dihydrochloride
Labeler
Meijer Distribution Inc
Marketing category
ANDA
Marketing start / end (source format)
20200206
Source listing expiry
20261231

Source-listed ingredients

  • LEVOCETIRIZINE DIHYDROCHLORIDE — 5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE in 1 CARTON (41250-488-01) / 35 TABLET, FILM COATED in 1 BOTTLE · 41250-488-01
  • 1 BOTTLE in 1 CARTON (41250-488-27) / 80 TABLET, FILM COATED in 1 BOTTLE · 41250-488-27

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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