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: 63868-151_08f2bf78-eba5-41ce-bcb0-733e2760d44b
Product NDC: 63868-151
Form: TABLET
Composition / generic term: Loratadine
Labeler: Chain Drug Marketing Association Inc.
Marketing category: ANDA
Marketing start / end (source format): 20030819
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 (63868-151-01) · 63868-151-01
10 TABLET in 1 BLISTER PACK (63868-151-10) · 63868-151-10
30 TABLET in 1 BLISTER PACK (63868-151-30) · 63868-151-30

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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