United States · FDA National Drug Code directory
Claritin-D 12 Hour
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
- 11523-7162_45371982-daab-f344-e063-6394a90a2f41
- Product NDC
- 11523-7162
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Loratadine and pseudoephedrine sulfate
- Labeler
- Bayer HealthCare LLC.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20091201
- Source listing expiry
- 20261231
Source-listed ingredients
- LORATADINE — 5 mg/1
- PSEUDOEPHEDRINE SULFATE — 120 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BLISTER PACK in 1 CARTON (11523-7162-1) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK · 11523-7162-1
- 2 BLISTER PACK in 1 CARTON (11523-7162-2) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK · 11523-7162-2
- 3 BLISTER PACK in 1 CARTON (11523-7162-3) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK · 11523-7162-3
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.
Browse United States records →