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
- 43598-183_9b5f0b11-2f7f-0cb0-0ce7-c06c0b85c5c7
- Product NDC
- 43598-183
- Form
- TABLET, FILM COATED
- Composition / generic term
- Cetirizine Hydrochloride Tablets
- Labeler
- Dr. Reddy's Laboratories Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20181217
- Source listing expiry
- 20261231
Source-listed ingredients
- CETIRIZINE HYDROCHLORIDE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 300 TABLET, FILM COATED in 1 BOTTLE (43598-183-31) · 43598-183-31
- 500 TABLET, FILM COATED in 1 BOTTLE (43598-183-55) · 43598-183-55
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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