United States · FDA National Drug Code directory
Cetirizine Hydrochloride (Allergy)
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
- 16714-799_31542c85-db9e-4225-bd25-d231710595b0
- Product NDC
- 16714-799
- Form
- TABLET
- Composition / generic term
- Cetirizine Hydrochloride
- Labeler
- NorthStar Rx LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20150805
- 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 (16714-799-01) · 16714-799-01
- 100 TABLET in 1 BOTTLE (16714-799-02) · 16714-799-02
- 300 TABLET in 1 BOTTLE (16714-799-03) · 16714-799-03
- 500 TABLET in 1 BOTTLE (16714-799-04) · 16714-799-04
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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