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
11523-7237_4536cd82-d67c-56be-e063-6294a90a7775
Product NDC
11523-7237
Form
TABLET
Composition / generic term
Loratadine
Labeler
Bayer HealthCare LLC.
Marketing category
NDA
Marketing start / end (source format)
19930412
Source listing expiry
20261231

Source-listed ingredients

  • LORATADINE — 10 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE in 1 CARTON (11523-7237-1) / 45 TABLET in 1 BOTTLE · 11523-7237-1
  • 7 BLISTER PACK in 1 CARTON (11523-7237-3) / 10 TABLET in 1 BLISTER PACK · 11523-7237-3
  • 1 BOTTLE in 1 BLISTER PACK (11523-7237-5) / 90 TABLET in 1 BOTTLE · 11523-7237-5
  • 3 BLISTER PACK in 1 CARTON (11523-7237-6) / 5 TABLET in 1 BLISTER PACK · 11523-7237-6
  • 4 BLISTER PACK in 1 CARTON (11523-7237-7) / 10 TABLET in 1 BLISTER PACK · 11523-7237-7
  • 1 BOTTLE in 1 CARTON (11523-7237-8) / 108 TABLET in 1 BOTTLE · 11523-7237-8
  • 1 BOTTLE in 1 CARTON (11523-7237-9) / 90 TABLET in 1 BOTTLE · 11523-7237-9

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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