United States · FDA National Drug Code directory

Desloratadine

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
55111-360_ae8e6303-9bd6-d6de-79d6-d70b7b736c96
Product NDC
55111-360
Form
TABLET, ORALLY DISINTEGRATING
Composition / generic term
Desloratadine
Labeler
Dr. Reddy's Laboratories Limited
Marketing category
ANDA
Marketing start / end (source format)
20130111
Source listing expiry
20261231

Source-listed ingredients

  • DESLORATADINE — 5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (55111-360-06) · 55111-360-06
  • 5 BLISTER PACK in 1 CARTON (55111-360-31) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK · 55111-360-31

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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Desloratadine — United States | Molindra Medicines