United States · FDA National Drug Code directory

LORATADINE

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
11822-7240_b93384f9-c93b-4ede-a8dc-c523c910bb2e
Product NDC
11822-7240
Form
TABLET, CHEWABLE
Composition / generic term
LORATADINE
Labeler
Rite Aid
Marketing category
ANDA
Marketing start / end (source format)
20180401
Source listing expiry
20261231

Source-listed ingredients

  • LORATADINE — 5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BLISTER PACK in 1 CARTON (11822-7240-0) / 30 TABLET, CHEWABLE in 1 BLISTER PACK · 11822-7240-0

Source and coverage

Open FDA National Drug Code directory

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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