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
82725-0142_42292076-863b-8cc2-e063-6294a90ae709
Product NDC
82725-0142
Form
TABLET
Composition / generic term
LORATADINE
Labeler
Cabinet Health P.B.C.
Marketing category
ANDA
Marketing start / end (source format)
20251001
Source listing expiry
20261231

Source-listed ingredients

  • LORATADINE — 10 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 8000 TABLET in 1 BAG (82725-0142-1) · 82725-0142-1
  • 1 BAG in 1 DRUM (82725-0142-2) / 100000 TABLET in 1 BAG · 82725-0142-2
  • 10000 TABLET in 1 BAG (82725-0142-3) · 82725-0142-3
  • 1 DRUM in 1 DRUM (82725-0142-4) / 96000 TABLET in 1 DRUM · 82725-0142-4

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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