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
- 71205-700_c5844e33-c337-4b62-91ca-de3d388b7d45
- Product NDC
- 71205-700
- Form
- TABLET
- Composition / generic term
- Cetirizine Hydrochloride
- Labeler
- Proficient Rx LP
- 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
- 100 TABLET in 1 BOTTLE (71205-700-00) · 71205-700-00
- 6 TABLET in 1 BOTTLE (71205-700-06) · 71205-700-06
- 10 TABLET in 1 BOTTLE (71205-700-10) · 71205-700-10
- 12 TABLET in 1 BOTTLE (71205-700-12) · 71205-700-12
- 14 TABLET in 1 BOTTLE (71205-700-14) · 71205-700-14
- 15 TABLET in 1 BOTTLE (71205-700-15) · 71205-700-15
- 20 TABLET in 1 BOTTLE (71205-700-20) · 71205-700-20
- 21 TABLET in 1 BOTTLE (71205-700-21) · 71205-700-21
- 30 TABLET in 1 BOTTLE (71205-700-30) · 71205-700-30
- 60 TABLET in 1 BOTTLE (71205-700-60) · 71205-700-60
- 120 TABLET in 1 BOTTLE (71205-700-72) · 71205-700-72
- 90 TABLET in 1 BOTTLE (71205-700-90) · 71205-700-90
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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