United States · FDA National Drug Code directory
Cetirizine Hydrochloride
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
- 63941-939_2d78941a-3bfd-4c92-aa00-2a4f99db44c8
- Product NDC
- 63941-939
- Form
- TABLET
- Composition / generic term
- Cetirizine Hydrochloride
- Labeler
- Valu Merchandisers Company
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20071227
- Source listing expiry
- 20261231
Source-listed ingredients
- CETIRIZINE HYDROCHLORIDE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (63941-939-30) · 63941-939-30
- 14 TABLET in 1 BLISTER PACK (63941-939-54) · 63941-939-54
- 60 TABLET in 1 BOTTLE (63941-939-60) · 63941-939-60
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 →