United States · FDA National Drug Code directory

LORATADINE ALLERGY RELIEF 10mg

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
73581-230_0e135981-fabe-f255-e063-6394a90ae356
Product NDC
73581-230
Form
TABLET
Composition / generic term
LORATADINE
Labeler
YYBA CORP
Marketing category
ANDA
Marketing start / end (source format)
20220415
Source listing expiry
20261231

Source-listed ingredients

  • LORATADINE — 10 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE (73581-230-01) · 73581-230-01
  • 365 TABLET in 1 BOTTLE (73581-230-36) · 73581-230-36

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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