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
- 71205-709_bb392ca5-d39d-4265-95b2-bc44e133101b
- Product NDC
- 71205-709
- Form
- TABLET, FILM COATED
- Composition / generic term
- Cetirizine Hydrochloride Tablets
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20181217
- Source listing expiry
- 20271231
Source-listed ingredients
- CETIRIZINE HYDROCHLORIDE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (71205-709-00) · 71205-709-00
- 6 TABLET, FILM COATED in 1 BOTTLE (71205-709-06) · 71205-709-06
- 10 TABLET, FILM COATED in 1 BOTTLE (71205-709-10) · 71205-709-10
- 20 TABLET, FILM COATED in 1 BOTTLE (71205-709-20) · 71205-709-20
- 30 TABLET, FILM COATED in 1 BOTTLE (71205-709-30) · 71205-709-30
- 90 TABLET, FILM COATED in 1 BOTTLE (71205-709-90) · 71205-709-90
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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