United States · FDA National Drug Code directory

Loratadine ODT

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
0363-9937_9bc8fa61-c4ea-477d-80ac-8c21c2fbd8ce
Product NDC
0363-9937
Form
TABLET, ORALLY DISINTEGRATING
Composition / generic term
Loratadine
Labeler
WALGREEN CO.
Marketing category
ANDA
Marketing start / end (source format)
20180411
Source listing expiry
20261231

Source-listed ingredients

  • LORATADINE — 10 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 3 BLISTER PACK in 1 CARTON (0363-9937-84) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK · 0363-9937-84

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.

Browse United States records →