United States · FDA National Drug Code directory
allergy relief D12
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
- 0363-4923_7b2562f7-d202-464a-a703-65d77a49031a
- Product NDC
- 0363-4923
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- Cetirizine hydrochloride, Pseudoephedrine hydrochloride
- Labeler
- Walgreen Company
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20211020
- Source listing expiry
- 20271231
Source-listed ingredients
- CETIRIZINE HYDROCHLORIDE — 5 mg/1
- PSEUDOEPHEDRINE HYDROCHLORIDE — 120 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 12 BLISTER PACK in 1 CARTON (0363-4923-53) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK · 0363-4923-53
- 24 BLISTER PACK in 1 CARTON (0363-4923-62) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK · 0363-4923-62
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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