United States · FDA National Drug Code directory
Allergy Relief
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
- 81522-194_2fc20c71-6615-68d4-e063-6294a90a736e
- Product NDC
- 81522-194
- Form
- TABLET, COATED
- Composition / generic term
- Cetirizine hydrochloride
- Labeler
- FSA STORE INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230111
- Source listing expiry
- 20261231
Source-listed ingredients
- CETIRIZINE HYDROCHLORIDE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, PLASTIC in 1 CARTON (81522-194-04) / 45 TABLET, COATED in 1 BOTTLE, PLASTIC · 81522-194-04
- 1 BOTTLE, PLASTIC in 1 CARTON (81522-194-16) / 90 TABLET, COATED in 1 BOTTLE, PLASTIC · 81522-194-16
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 →