United States · FDA National Drug Code directory
Loratadine and Pseudoephedrine
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
- 0363-0725_0c2d87ca-fff0-46d5-9800-756693969a77
- Product NDC
- 0363-0725
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- Loratadine and Pseudoephedrine
- Labeler
- Walgreen Company
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20131107
- Source listing expiry
- 20261231
Source-listed ingredients
- LORATADINE — 10 mg/1
- PSEUDOEPHEDRINE SULFATE — 240 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BLISTER PACK in 1 CARTON (0363-0725-15) / 15 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK · 0363-0725-15
- 1 BLISTER PACK in 1 CARTON (0363-0725-56) / 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK · 0363-0725-56
- 1 BLISTER PACK in 1 CARTON (0363-0725-69) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK · 0363-0725-69
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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