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
- 70677-1007_b13a3e2a-c087-727c-8d9e-90faa85292e6
- Product NDC
- 70677-1007
- Form
- TABLET, FILM COATED
- Composition / generic term
- Cetirizine Hydrochloride Tablets
- Labeler
- Strategic Sourcing Services LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220512 / 20270228
Source-listed ingredients
- CETIRIZINE HYDROCHLORIDE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (70677-1007-2) / 60 TABLET, FILM COATED in 1 BOTTLE · 70677-1007-2
- 1 BOTTLE in 1 CARTON (70677-1007-3) / 90 TABLET, FILM COATED in 1 BOTTLE · 70677-1007-3
- 1 BOTTLE in 1 CARTON (70677-1007-4) / 300 TABLET, FILM COATED in 1 BOTTLE · 70677-1007-4
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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