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
- 55111-551_ae8e6303-9bd6-d6de-79d6-d70b7b736c96
- Product NDC
- 55111-551
- 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 — 2.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (55111-551-06) · 55111-551-06
- 5 BLISTER PACK in 1 CARTON (55111-551-31) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK · 55111-551-31
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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