United States · FDA National Drug Code directory
Allergy relief-D
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
- 51660-940_767603f0-b735-4513-97d9-6c69a0bf70e3
- Product NDC
- 51660-940
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride
- Labeler
- Ohm Laboratories Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170502
- Source listing expiry
- 20261231
Source-listed ingredients
- CETIRIZINE HYDROCHLORIDE — 5 mg/1
- PSEUDOEPHEDRINE HYDROCHLORIDE — 120 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 2 BLISTER PACK in 1 CARTON (51660-940-12) / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK · 51660-940-12
- 4 BLISTER PACK in 1 CARTON (51660-940-24) / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK · 51660-940-24
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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