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
- 63941-526_bc05aca7-4224-4b42-93b7-d28fbf18c0b1
- Product NDC
- 63941-526
- Form
- TABLET
- Composition / generic term
- Loratadine
- Labeler
- Valu Merchandisers Company
- 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
- 30 TABLET in 1 BLISTER PACK (63941-526-31) · 63941-526-31
- 60 TABLET in 1 BOTTLE (63941-526-60) · 63941-526-60
- 10 TABLET in 1 BLISTER PACK (63941-526-69) · 63941-526-69
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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