United States · FDA National Drug Code directory
Allergy Relief
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
- 68998-194_ea60a2f4-2e8f-c1f1-e053-2a95a90a286a
- Product NDC
- 68998-194
- Form
- TABLET, COATED
- Composition / generic term
- Cetirizine hydrochloride
- Labeler
- MARC GLASSMAN, INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200301
- Source listing expiry
- 20261231
Source-listed ingredients
- CETIRIZINE HYDROCHLORIDE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, PLASTIC in 1 CARTON (68998-194-02) / 30 TABLET, COATED in 1 BOTTLE, PLASTIC · 68998-194-02
- 1 BOTTLE, PLASTIC in 1 CARTON (68998-194-07) / 90 TABLET, COATED in 1 BOTTLE, PLASTIC · 68998-194-07
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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