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
54838-554_fd40a94c-2173-4b80-a049-ab3c4faf24f4
Product NDC
54838-554
Form
SOLUTION
Composition / generic term
Loratadine
Labeler
Lannett Company, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20101124
Source listing expiry
20261231

Source-listed ingredients

  • LORATADINE — 5 mg/5mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 120 mL in 1 CARTON (54838-554-40) · 54838-554-40

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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