United States · FDA National Drug Code directory

Allergy Relief

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
68998-414_ad095cf5-0a18-4a1f-8881-b6b2cd4fa1f7
Product NDC
68998-414
Form
TABLET
Composition / generic term
Loratadine
Labeler
Marc Glassman, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20200501
Source listing expiry
20261231

Source-listed ingredients

  • LORATADINE — 10 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 90 TABLET in 1 BOTTLE (68998-414-82) · 68998-414-82
  • 30 TABLET in 1 CARTON (68998-414-85) · 68998-414-85

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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