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
- 83324-009_fc49fe88-56a3-6dcf-e053-6294a90adb84
- Product NDC
- 83324-009
- Form
- TABLET
- Composition / generic term
- Fexofenadine Hydrochloride
- Labeler
- Chain Drug Marketing Association, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230522
- Source listing expiry
- 20261231
Source-listed ingredients
- FEXOFENADINE HYDROCHLORIDE — 60 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BLISTER PACK in 1 CARTON (83324-009-12) / 12 TABLET in 1 BLISTER PACK · 83324-009-12
- 2 BLISTER PACK in 1 CARTON (83324-009-24) / 12 TABLET in 1 BLISTER PACK · 83324-009-24
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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