United States · FDA National Drug Code directory

Claritin

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
11523-0007_4526b265-4250-3e71-e063-6294a90a21a8
Product NDC
11523-0007
Form
TABLET
Composition / generic term
loratadine
Labeler
Bayer HealthCare LLC.
Marketing category
ANDA
Marketing start / end (source format)
20201201
Source listing expiry
20261231

Source-listed ingredients

  • LORATADINE — 10 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BLISTER PACK in 1 CARTON (11523-0007-1) / 10 TABLET in 1 BLISTER PACK · 11523-0007-1
  • 2 BLISTER PACK in 1 CARTON (11523-0007-2) / 10 TABLET in 1 BLISTER PACK · 11523-0007-2
  • 30 TABLET in 1 BOTTLE (11523-0007-3) · 11523-0007-3
  • 40 TABLET in 1 BOTTLE (11523-0007-4) · 11523-0007-4
  • 45 TABLET in 1 BOTTLE (11523-0007-5) · 11523-0007-5
  • 70 TABLET in 1 BOTTLE (11523-0007-6) · 11523-0007-6
  • 85 TABLET in 1 BOTTLE (11523-0007-7) · 11523-0007-7
  • 2 BOTTLE in 1 CARTON (11523-0007-8) / 115 TABLET in 1 BOTTLE · 11523-0007-8
  • 60 TABLET in 1 BOTTLE (11523-0007-9) · 11523-0007-9

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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