United States · FDA National Drug Code directory
Cetirizine
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
- 83939-0003_43f4168a-615f-a724-e063-6394a90a24b6
- Product NDC
- 83939-0003
- Form
- TABLET, FILM COATED
- Composition / generic term
- Cetirizine Hydrochloride
- Labeler
- VERITYRX, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20251103
- Source listing expiry
- 20261231
Source-listed ingredients
- CETIRIZINE HYDROCHLORIDE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 50 POUCH in 1 BOX, UNIT-DOSE (83939-0003-0) / 1 TABLET, FILM COATED in 1 POUCH · 83939-0003-0
- 50 POUCH in 1 BOX, UNIT-DOSE (83939-0003-2) / 1 TABLET, FILM COATED in 1 POUCH · 83939-0003-2
- 100 POUCH in 1 BOX, UNIT-DOSE (83939-0003-3) / 1 TABLET, FILM COATED in 1 POUCH · 83939-0003-3
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 →